Project/Premed/Syllabus

COMPLETE CURRICULUM · VERSION 1.0 CANDIDATE

Premed syllabus

Common curriculum
1,440h
Pathway
120–240h
Sections
24 + appendices

The complete academic contract: audience, entry, outcomes, every module and topic, pathways, practicals, assessment, remediation, schedules, resources, quality assurance, and boundaries.

All sections visible.

Premed: Foundations for Medical Study

Curriculum version: 1.1 candidate · 20 July 2026
Provider: EmbeddedKnowledge
Language: English
Level: university preparatory; introductory undergraduate science with a medicine-facing bridge
Format: mastery-based, online-first, asynchronous with optional live/tutorial and supervised practical components
Nominal workload: 1,440 hours for the common core and medicine bridge, plus 120–240 hours for one pathway
Typical pace: 72 weeks at 22–24 hours/week; 96 weeks at 17–18 hours/week part-time; no fixed expiry
Credential: an EmbeddedKnowledge record of demonstrated outcomes, not a university degree, academic credit, professional license, medical-school admission guarantee, or substitute for institution-specific prerequisites

Course promise: finishers should be able to explain, model, investigate, and integrate the science that a well-prepared entrant commonly brings to medical study. The target is demonstrated readiness, not merely exposure and not an admissions credential.

1. Place in the curriculum#

Premed is EmbeddedKnowledge's first course and the prerequisite for later medical-science courses. It deliberately combines the portable scientific spine found across major preparation systems with a clearly labelled medicine-facing bridge and route-specific pathways.

It does not claim that every medical entrant in every country has taken all of these subjects. Admissions requirements are decentralized in the United States, institution-specific in the United Kingdom, and partly determined by annual university weightings in Spain. AP, IB, A-level, Bachillerato, Abitur, and Baccalaureat subject lists are choices or curriculum unions, not a single global entrant minimum. A learner applying to a real institution must check that institution's current rules.

The course is broader than the MCAT where medical readiness benefits from anatomy, physiology, immunity, laboratory practice, and scientific communication. It is narrower than a biology degree: ecology, plant biology, calculus-based physics, and advanced organic synthesis are pathway options rather than universal requirements.

2. Audience#

Premed is designed for:

  • curious adults who want genuine premedical knowledge without seeking a title;
  • prospective medical applicants who need a structured foundation or route-specific review;
  • nurses, EMTs, biomedical engineers, health-technology workers, and other health-adjacent learners filling gaps;
  • access/foundation learners rebuilding mathematics, chemistry, biology, or academic-English confidence.

No prior degree is required. The normal entry floor is upper-secondary reading and algebra. Prior science courses may shorten the route through diagnostic placement; they never exempt a learner from demonstrating the mapped outcomes.

3. Entry, diagnostic placement, and on-ramp#

3.1 Expected entry capabilities#

Before the common core, learners should be able to:

  • read a 1,000-word expository text and state its claim and supporting evidence;
  • rearrange a one-variable equation, use fractions, ratios, percentages, and powers of ten;
  • interpret axes, slope, and a simple data table;
  • use a calculator and basic spreadsheet cells without copying sensitive data to a public service;
  • write a short explanation in their own words and distinguish a quotation from a paraphrase;
  • follow basic digital-safety and laboratory-safety instructions.

3.2 Diagnostic#

The untimed entry diagnostic has five 30–45 minute stations: DIA-MATH, DIA-READ, DIA-CHEM, DIA-BIO, and DIA-DATA. It samples prerequisites only; it is not graded. Each station produces a concept-level placement report and one of three actions:

Result Action
Secure (at least 85%, no critical misconception) Begin the linked core node; on-ramp practice remains available.
Developing (60–84%) Complete only the prescribed on-ramp lessons and retry the station.
Foundational (below 60% or a critical safety/numeracy error) Complete the full on-ramp below with tutor check-ins.

3.3 On-ramp ONR-000 (0–120 hours, as needed)#

Topic ID Scope Exit evidence
ONR-001 Scientific language variables, units, prefixes, notation, estimation, significant figures annotate and calculate from a short scientific passage
ONR-002 Algebra equations, inequalities, ratios, proportionality, exponents, scientific notation solve a mixed, contextual problem set with units
ONR-003 Graphs and functions linear, inverse, exponential, logarithmic relationships; interpolation construct and interpret three graph types
ONR-004 Chemical language element symbols, formulas, ions, moles as counting units translate words, formulas, and particle diagrams
ONR-005 Cell and gene primer cells, chromosomes, genes, proteins, energy as orienting models produce a correct concept map without memorized detail
ONR-006 Evidence and reading claims, evidence, assumptions, correlation, causation, source types critique a short popular-health claim
ONR-007 Study system retrieval practice, spacing, interleaving, error logs, planning run a two-week study cycle and reflect on its data
ONR-008 Academic English paragraph logic, disciplinary vocabulary, paraphrase, discussion norms submit a cited 500-word explanation

Learners may use another language to reason or annotate, but assessed scientific terms and final explanations are in English. Accommodations are described in section 16.

4. Curriculum philosophy#

  1. A knowledge graph, not a content pile. Every topic has a stable ID, prerequisites, observable outcomes, evidence, and downstream uses.
  2. Reasoning is the curriculum. Recall supports modelling, experimental design, data analysis, and argument. It never substitutes for them.
  3. Mastery is revisable. Gates are untimed and retakeable after targeted practice. A failed attempt is diagnostic evidence, not a verdict.
  4. Medicine supplies context, not false authority. Cases make basic science consequential, but learners do not diagnose, prescribe, or simulate clinical competence.
  5. Representations must agree. Learners move among words, equations, graphs, mechanisms, diagrams, and physical models.
  6. Practical evidence matters. Simulations can teach design and interpretation; they cannot prove hands-on dexterity. The record names which modality was actually completed.
  7. Sources outrank confidence. Claims are traceable. Uncertainty, limitations, and correction are normal parts of scholarship.
  8. Motivation is infrastructure. Visible node-level progress, short feedback loops, learner choice, recovery weeks, and meaningful cases are core design requirements.

5. Program-level learning outcomes#

By completion, a learner can:

Knowledge and explanation#

  1. PLO-01 Explain how atomic and molecular interactions give rise to biological structure, reactivity, energy transfer, and measurement.
  2. PLO-02 Explain cells as regulated, evolving systems that exchange matter, energy, and information.
  3. PLO-03 Trace genetic information from inheritance through gene expression and connect variation to phenotype.
  4. PLO-04 Model enzyme function, bioenergetics, and the integration and regulation of major metabolic pathways.
  5. PLO-05 Apply introductory organic chemistry to biologically important functional groups, stereochemistry, mechanisms, and analytical evidence.
  6. PLO-06 Apply algebra-based mechanics, fluids, thermal physics, electricity, waves, optics, and atomic/nuclear physics to biological and medical contexts.
  7. PLO-07 Explain homeostasis through integrated organ-system structure, transport, control, and feedback.
  8. PLO-08 Explain host defence, microbial and viral strategies, biotechnology, and the limits and ethics of intervention.

Inquiry and quantitative reasoning#

  1. PLO-09 Form a testable question, identify variables and controls, select measurements, anticipate confounding, and distinguish exploratory from confirmatory work.
  2. PLO-10 Calculate with units, uncertainty, ratios, logarithms, probability, descriptive statistics, confidence intervals, and simple inferential tests at the course's stated level.
  3. PLO-11 Create and interpret tables, graphs, images, spectra, and simple models without overstating what the data establish.
  4. PLO-12 Evaluate validity, reliability, bias, effect size, statistical versus practical significance, and alternative explanations.
  5. PLO-13 Keep a reproducible record, handle data ethically, and communicate methods sufficiently for another learner to audit the work.

Integration, communication, and self-regulation#

  1. PLO-14 Integrate chemistry, biology, physics, and behaviour in unfamiliar medicine-facing problems while distinguishing mechanism from association.
  2. PLO-15 Read a primary research article at an introductory level and reconstruct its question, method, principal result, limitations, and warranted conclusion.
  3. PLO-16 Explain a scientific idea accurately to expert and public audiences, cite sources, disclose tool use, and revise after critique.
  4. PLO-17 Identify the boundary between education and medical advice and recognize when a claim requires a qualified professional.
  5. PLO-18 Use retrieval data, confidence calibration, an error taxonomy, and a study plan to remediate weak nodes independently.

Route-specific outcomes (PLO-US, PLO-UK, PLO-ES, PLO-BIO, and PLO-QNT) are defined in section 12.

6. Architecture and completion rules#

6.1 Components#

Component Modules Nominal hours Required for EmbeddedKnowledge Premed completion?
Course welcome WEL-000 1 Yes
On-ramp ONR-000 0–120 Only when prescribed by diagnostic
Inquiry and quantitative spine QRS-100, embedded studios 180 Yes
General chemistry CHE-110CHE-140 220 Yes
Biology and genetics BIO-110BIO-150 250 Yes
Physics PHY-110PHY-150 210 Yes
Organic chemistry ORG-210ORG-230 150 Yes
Biochemistry BCH-210BCH-240 200 Yes
Medicine-facing bridge MED-310MED-330 170 Yes, but labelled as EmbeddedKnowledge design scope rather than universal entrant minimum
Integration and capstone INT-300, CAP-400 60 Yes
One route/pathway section 12 120–240 Yes; learner may complete more than one

Hours overlap because inquiry studios, practical work, retrieval, and cases are embedded in disciplinary modules. The common-core plus bridge total is capped at 1,440 nominal hours, not the sum of every possible activity in every row.

6.2 Completion standard#

Completion requires all of the following:

  • every required outcome at M (mastered) or above in the mastery ledger;
  • all safety-critical outcomes at M with no compensation by average;
  • twelve practical investigations, including at least four using physical equipment if the learner wants a blended-practical notation;
  • the research-reading portfolio and quantitative portfolio;
  • one completed route/pathway (see the instrumentation limitation in section 12: in curriculum version 1.1 only PW-US, PW-BIO and PW-QNT can satisfy this requirement, because PW-UK and PW-ES are not yet represented in the knowledge graph);
  • an accepted integrative capstone and oral defence;
  • a final calibration review showing that confidence judgments track actual performance.

No time limit applies. Institution-specific applications may require formally accredited laboratory courses regardless of this record.

7. Stable mastery language#

Each outcome is stored independently; module averages cannot hide a gap.

State Meaning Minimum evidence
N Not yet encountered No interpretable evidence none
A Acquiring Can follow a worked example; recall is fragile guided checks
P Practising Can solve familiar problems with limited prompts two successful practice occasions
M Mastered Can explain and apply independently in a new but bounded context gate at ≥80%, all critical items correct, plus transfer task
R Retained Re-demonstrated after spacing in a different context two delayed checks, one at least 21 days later
T Transfer Uses the outcome appropriately in a cross-domain case or investigation rubric-scored authentic task

Confidence is logged before feedback on selected tasks. A high-confidence incorrect response triggers misconception remediation even if the surrounding module score is adequate.

8. Module sequence at a glance#

Modules are shown in the recommended order. || indicates modules that can run concurrently after their shared prerequisites.

WEL-000
  -> QRS-100 (begins with Scientific Inquiry)
  -> CHE-110 || BIO-110
  -> CHE-120 || BIO-120 || PHY-110
  -> CHE-130 || BIO-130 || PHY-120
  -> CHE-140 || BIO-140 || PHY-130
  -> ORG-210 || BIO-150 || PHY-140
  -> ORG-220 || BCH-210 || PHY-150
  -> ORG-230 || BCH-220
  -> BCH-230 -> BCH-240
  -> MED-310 || MED-320 -> MED-330
  -> INT-300 + one PATHWAY
  -> CAP-400

WEL-000 is the only lesson before the scientific curriculum. It previews the complete journey and the capabilities learners are working toward. QRS-100 then opens with Scientific Inquiry; its practices continue through every later module. Diagnostic-prescribed ONR-000 refreshers are optional support, not a separate opening content block. The curriculum map in PREMED-CURRICULUM-MAP.md gives the cross-domain edges and misconception gates.

9. Detailed common-core modules#

WEL-000 Welcome to Premed — 1 hour#

Purpose. Welcome learners into the scientific journey ahead before asking them to master any new content. The lesson previews the questions each subject helps answer, shows how the subjects connect, and makes the destination concrete: by the end, learners should be able to explain, model, investigate, and integrate the science that supports later medical study.

The welcome introduces the course in plain language:

  • Scientific inquiry and laboratory practice: how we turn a question into a fair test, decide what evidence can support, and make work reproducible.
  • Mathematics, statistics, chemistry, and physics: how we measure the world and explain matter, energy, forces, fluids, electricity, waves, and uncertainty.
  • Biology, genetics, organic chemistry, and biochemistry: how cells are built, use energy, store information, respond, reproduce, and change.
  • Human systems, immunity, microbiology, behaviour, and society: how those foundations connect across a whole person and population without pretending that premedical study is clinical practice.
  • Integration and capstones: how learners will combine the subjects to reason through unfamiliar problems rather than merely repeat isolated facts.

Completion evidence. The learner can describe the subject journey, explain why its major concepts matter for medical study, and identify what they should know and be able to do by course completion. This is a motivating orientation, not a prior-knowledge test or a graded science gate.

QRS-100 Quantitative and scientific reasoning — 180 hours distributed#

Purpose. Begin with Scientific Inquiry—questions, hypotheses, variables, evidence, causal limits, uncertainty, and reproducibility—then establish the mathematical and statistical practices used everywhere else.

Instruction begins with QRS-105, QRS-110, and QRS-112; the numeric IDs below are stable references, not a required teaching order. Laboratory and measurement work then make the inquiry cycle concrete before the remaining quantitative sequence expands what learners can test and interpret.

Topic ID Topic-level scope and measurable outcome
QRS-101 Dimensions and estimation: convert units, check dimensional consistency, propagate powers of ten, estimate order of magnitude, and explain whether a result is physically plausible.
QRS-102 Algebraic models: solve and rearrange linear, inverse, proportional, power, exponential, and logarithmic relationships; state domain assumptions.
QRS-103 Functions and graphs: derive slope and area meanings in context; recognize linearized relationships; choose axes and scales that do not mislead.
QRS-104 Measurement: distinguish accuracy, precision, resolution, random error, systematic error, calibration, and uncertainty; report significant figures appropriately.
QRS-105 Study design: distinguish observational, experimental, cross-sectional, case-control, cohort, and randomized designs at an introductory level; identify exposure, outcome, controls, blinding, randomization, and confounding.
QRS-106 Descriptive statistics: compute and interpret mean, median, variance, standard deviation, percentile, distribution shape, outlier, and standardization.
QRS-107 Probability: use complements, conditional probability, independence, counting, Bayes reasoning with natural frequencies, sensitivity, specificity, and predictive values.
QRS-108 Inference: interpret sampling variability, confidence intervals, null hypotheses, p-values, Type I/II errors, power, effect sizes, correlation, simple linear regression, chi-square, and a two-group comparison without treating a p-value as truth. Calculation emphasis is limited to simple hand/spreadsheet cases.
QRS-109 Data representation: construct and critique tables, scatterplots, line/bar plots, histograms, box plots, uncertainty bars, log plots, and image quantification.
QRS-110 Causal and model reasoning: distinguish association from causation, mechanism from prediction, model from reality, and interpolation from extrapolation; compare plausible alternatives.
QRS-111 Evidence appraisal: reconstruct a paper's question, population, design, result, limitation, funding/conflict disclosure, and warranted claim.
QRS-112 Reproducible practice: maintain a dated notebook, data dictionary, formulas or scripts, provenance, change log, and an auditable figure.

Activities and evidence. Weekly mixed quantitative sets; misleading-graph repair; diagnostic-test natural-frequency simulation; paper figure reconstruction; preregistration of one miniature investigation; reproducibility audit by a peer or tutor.

Mastery gate. An unseen multi-figure study requiring calculations, design critique, uncertainty analysis, and a 700-word evidence judgment. Safety-critical items are unit conversion, denominator choice, and unsupported causal claims.

Deliberate exclusions. Calculus, matrix algebra, ANOVA derivations, multivariable regression, survival analysis, and programming proficiency are not in the common core. They appear only in PW-QNT or later medical research courses.


CHE-110 Matter, measurement, atoms, and periodicity — 50 hours#

Prerequisites: QRS-101QRS-104.

Topic ID Scope and outcome
CHE-111 Classify matter, physical/chemical properties, and changes; select separation methods from particle-level reasoning.
CHE-112 Use SI quantities, density, temperature scales, uncertainty, and significant figures in laboratory calculations.
CHE-113 Relate protons, neutrons, electrons, isotopes, ions, atomic mass, and mole-scale measurements.
CHE-114 Use electromagnetic radiation and quantized-energy evidence to describe atomic orbitals and electron configurations at introductory depth.
CHE-115 Predict periodic trends in radius, ionization energy, electron affinity, and electronegativity and justify exceptions cautiously.
CHE-116 Name and formulate common ionic and molecular compounds; move among symbolic, macroscopic, and particulate representations.

Practice/practical. Density and calibration investigation; isotope-abundance problem set; flame/emission-spectrum simulation or supervised demonstration.

Gate. Identify an unknown material from measurement and spectroscopic evidence and defend the uncertainty budget.

Exclusions. Full quantum-mechanical derivations and many-electron wavefunctions.

BIO-110 Chemistry of life and cellular organization — 55 hours#

Prerequisites: CHE-111CHE-116 may be co-studied.

Topic ID Scope and outcome
BIO-111 Relate water polarity, hydrogen bonding, ions, hydrophobic effects, pH, and buffering to biological environments.
BIO-112 Compare carbohydrates, lipids, proteins, and nucleic acids by monomer, bond, structure, function, and chemical behavior.
BIO-113 Explain prokaryotic and eukaryotic cell organization, organelles, surface-area constraints, and endosymbiotic evidence.
BIO-114 Explain membrane structure, fluidity, diffusion, osmosis, channels, carriers, pumps, and electrochemical gradients.
BIO-115 Predict effects of extracellular tonicity and transport disruption from concentration and permeability data.
BIO-116 Explain cytoskeleton, extracellular matrix, junctions, adhesion, and cell motility as dynamic systems.
BIO-117 Relate microscopy choice, scale bars, magnification, resolution, staining, and artifacts to a biological claim.

Practice/practical. Membrane permeability investigation; microscopy/image-scale lab; osmotic model; biomolecule evidence stations.

Gate. Explain an unfamiliar transport disorder from molecular, cellular, and quantitative evidence.

Exclusions. Named rare storage diseases and exhaustive organelle protein inventories.

CHE-120 Bonding, reactions, and stoichiometry — 55 hours#

Prerequisites: CHE-110, QRS-102.

Topic ID Scope and outcome
CHE-121 Draw and evaluate Lewis structures, formal charge, resonance, VSEPR geometry, polarity, and hybridization as useful models.
CHE-122 Relate ionic, covalent, metallic bonding and intermolecular forces to structure and measurable properties.
CHE-123 Balance equations and classify precipitation, acid-base, gas-forming, redox, and combustion reactions.
CHE-124 Convert among mass, moles, particles, concentration, gas volume, and equivalents with correct units.
CHE-125 Solve limiting-reagent, theoretical/percent-yield, empirical/molecular-formula, and mixture problems.
CHE-126 Write complete and net ionic equations and predict solubility using supplied rules and particle reasoning.

Practice/practical. Gravimetric or microscale precipitation investigation; solution preparation; reaction-yield audit.

Gate. Plan, calculate, execute or simulate, and audit a microscale synthesis with limiting reagent and uncertainty.

Exclusions. Industrial process engineering and advanced crystallography.

BIO-120 Cell energy, enzymes, signalling, and division — 55 hours#

Prerequisites: BIO-110, CHE-120 co-study recommended.

Topic ID Scope and outcome
BIO-121 Distinguish energy, free-energy change, activation energy, equilibrium, and coupling in cellular terms.
BIO-122 Explain enzyme active sites, specificity, saturation, environmental effects, inhibition, allostery, and feedback regulation using rate data.
BIO-123 Trace cellular respiration conceptually through glycolysis, pyruvate oxidation, citric-acid cycle, electron transport, chemiosmosis, and fermentation. Detailed integration follows in biochemistry.
BIO-124 Compare receptor classes and trace a signal through transduction, amplification, response, termination, and cross-talk.
BIO-125 Explain cell-cycle control, mitosis, checkpoints, apoptosis, stem-cell renewal, and how loss of regulation contributes to cancer.
BIO-126 Compare meiosis and mitosis and connect chromosome behavior to variation and aneuploidy.

Practice/practical. Enzyme kinetics investigation; mitotic-index image analysis; signalling-pathway perturbation model.

Gate. Interpret enzyme and cell-cycle experiments, then propose a discriminating follow-up.

Exclusions. Memorization of every signalling intermediate and clinical oncology management.

PHY-110 Motion, forces, energy, and momentum — 55 hours#

Prerequisites: QRS-101QRS-103.

Topic ID Scope and outcome
PHY-111 Represent vectors and one-/two-dimensional motion using diagrams, equations, and position/velocity/acceleration graphs.
PHY-112 Construct free-body diagrams and apply Newton's laws, friction, tension, normal force, gravity, and circular-motion relations.
PHY-113 Apply work, kinetic/potential energy, power, conservation, and efficiency to bounded systems.
PHY-114 Apply impulse and linear-momentum conservation; distinguish elastic and inelastic collisions.
PHY-115 Use torque, centre of mass, equilibrium, and mechanical advantage in simple biomechanical models.
PHY-116 Evaluate assumptions in idealized movement and injury models rather than mistaking the model for clinical prediction.

Practice/practical. Video motion analysis; force/lever model of a limb; conservation simulation; uncertainty in derived acceleration.

Gate. Build and validate an algebra-based mechanical model from an unfamiliar movement dataset.

Exclusions. Calculus derivations, rigid-body tensors, continuum mechanics, and diagnosis of injury.

CHE-130 States, gases, solutions, and thermochemistry — 55 hours#

Prerequisites: CHE-120, PHY-110 may be concurrent.

Topic ID Scope and outcome
CHE-131 Use kinetic-molecular theory and phase diagrams to explain states, phase change, vapour pressure, and deviations from idealization.
CHE-132 Apply gas laws, partial pressures, mole fractions, and gas stoichiometry to laboratory and respiratory contexts.
CHE-133 Prepare and dilute solutions; calculate molarity, molality, mass fraction, and selected colligative effects.
CHE-134 Explain dissolution using intermolecular interactions and energy/entropy tradeoffs; predict qualitative solubility.
CHE-135 Apply system/surroundings, heat, work, calorimetry, enthalpy, Hess's law, and bond-energy estimates.
CHE-136 Distinguish enthalpy, entropy, and Gibbs free energy and connect spontaneity to conditions without implying rate.

Practice/practical. Calorimetry; dilution and standard-curve preparation; gas-law simulation with residual analysis.

Gate. Quantitatively explain a coupled gas/solution/thermal process and evaluate model failure.

Exclusions. Real-gas equations beyond qualitative deviations and statistical thermodynamics.

BIO-130 Heredity, chromosomes, and populations — 45 hours#

Prerequisites: BIO-120, probability portions of QRS-107.

Topic ID Scope and outcome
BIO-131 Use Mendelian models, pedigrees, test crosses, and probability while recognizing model assumptions.
BIO-132 Analyze incomplete dominance, codominance, multiple alleles, penetrance, expressivity, linkage, recombination, and sex linkage.
BIO-133 Explain chromosomal segregation, nondisjunction, structural variation, genomic imprinting at survey depth, and karyotype evidence.
BIO-134 Apply Hardy-Weinberg as a null model and reason about mutation, selection, drift, migration, and non-random mating.
BIO-135 Explain natural selection, adaptation, common ancestry, and speciation using multiple lines of evidence without teleological language.
BIO-136 Distinguish individual risk, family recurrence, population frequency, and causal determinism in genetic communication.

Practice/practical. Model-organism or simulated crosses; chi-square analysis; pedigree critique; allele-frequency simulation.

Gate. Reconcile molecular, pedigree, and population data for an unfamiliar trait and communicate uncertainty.

Exclusions. Clinical genetic counselling, polygenic risk-score construction, ecology, and detailed phylogenetic computation.

PHY-120 Fluids, solids, and transport — 40 hours#

Prerequisites: PHY-110, CHE-130 recommended.

Topic ID Scope and outcome
PHY-121 Apply density, pressure, hydrostatic pressure, Pascal's principle, buoyancy, and continuity.
PHY-122 Use Bernoulli reasoning with explicit assumptions and recognize where viscosity invalidates it.
PHY-123 Relate laminar flow, resistance, radius, viscosity, and pressure gradient qualitatively and with supplied equations.
PHY-124 Explain surface tension, capillarity, adhesion/cohesion, and their biological implications.
PHY-125 Interpret stress, strain, elastic modulus, and failure in simplified tissue/material models.

Practice/practical. Flow-resistance investigation with tubing; pressure sensor or simulation; capillary measurement.

Gate. Evaluate a model of flow through a branching system, including assumptions and sensitivity to radius.

Exclusions. Full Navier-Stokes derivation, turbulence modelling, and hemodynamic diagnosis.

CHE-140 Kinetics, equilibrium, acids/bases, and electrochemistry — 60 hours#

Prerequisites: CHE-130, QRS-102.

Topic ID Scope and outcome
CHE-141 Determine and interpret rate, rate law, reaction order, integrated-rate graphs at introductory depth, half-life, collision factors, catalysts, and multi-step energy profiles.
CHE-142 Apply dynamic equilibrium, reaction quotient, equilibrium constants, and Le Chatelier reasoning while distinguishing kinetics from position.
CHE-143 Define acids and bases using Brønsted-Lowry and Lewis models; identify conjugate pairs, amphoterism, and relative strength.
CHE-144 Calculate pH/pOH for strong species and bounded weak-acid/base systems; use Ka, Kb, pKa, percent ionization, and approximations responsibly.
CHE-145 Explain buffers, Henderson-Hasselbalch use and limits, titration curves, indicators, equivalence, and physiological acid-base context without clinical interpretation.
CHE-146 Assign oxidation states, balance introductory redox reactions, and relate galvanic/electrolytic cells, potential, free energy, and concentration qualitatively or with supplied equations.
CHE-147 Apply solubility equilibria, common-ion effects, complexation at survey depth, and competing equilibria in qualitative analysis.

Practice/practical. Reaction-rate investigation; pH-metric titration and buffer-capacity comparison; electrochemical cell or simulation; open-response equilibrium defence.

Gate. Investigate an unknown acid/base system and integrate rate, equilibrium, uncertainty, and molecular explanation.

Exclusions. Full activity-coefficient treatment, advanced electroanalytical chemistry, and clinical management of acid-base disorders.

BIO-140 Molecular biology and control of gene expression — 55 hours#

Prerequisites: BIO-130, CHE-140 may be concurrent.

Topic ID Scope and outcome
BIO-141 Explain DNA/RNA structure, antiparallel organization, base pairing, chromatin, and genome organization.
BIO-142 Trace replication, repair, mutation, telomere function, and evidence for semiconservative replication at introductory depth.
BIO-143 Trace transcription, RNA processing, the genetic code, translation, protein targeting, and degradation.
BIO-144 Compare prokaryotic and eukaryotic gene regulation and reason from promoter, enhancer, transcription-factor, epigenetic, and RNA-level perturbations.
BIO-145 Predict molecular and phenotypic consequences of substitution, insertion/deletion, splice, regulatory, and copy-number changes.
BIO-146 Explain PCR, electrophoresis, restriction analysis, sequencing, cloning, recombinant expression, and CRISPR-Cas systems by purpose, inputs, outputs, controls, and limitations.
BIO-147 Evaluate the evidence and ethical dimensions of a bounded genetic-technology proposal without assuming that technical feasibility determines acceptability.

Practice/practical. DNA extraction; PCR/electrophoresis simulation or supervised wet lab; sequence alignment; gene-expression dataset; CRISPR claim audit.

Gate. Select and defend a molecular strategy to test an unfamiliar gene-function claim, including controls and ethical limits.

Exclusions. Production-scale bioinformatics, genome assembly, clinical variant classification, and therapeutic recommendations.

PHY-130 Oscillations, waves, sound, and optics — 45 hours#

Prerequisites: PHY-110, QRS-102QRS-103.

Topic ID Scope and outcome
PHY-131 Relate period, frequency, amplitude, wavelength, speed, phase, energy, and superposition in oscillations and waves.
PHY-132 Explain interference, standing waves, resonance, damping, reflection, refraction, and diffraction with diagrams and bounded calculations.
PHY-133 Apply intensity, inverse-square behavior, decibel scale, pitch, timbre, Doppler effect, and ultrasound principles.
PHY-134 Use ray models for mirrors, thin lenses, focal length, image formation, and magnification.
PHY-135 Explain refraction, total internal reflection, dispersion, polarization at survey depth, and optical instrument resolution.
PHY-136 Connect wave/optics models to hearing, vision, microscopy, fibre optics, and imaging while identifying where physiology or engineering adds complexity.

Practice/practical. Resonance measurement; decibel/logarithm task; lens focal-length and uncertainty investigation; optical-system ray tracing.

Gate. Design or evaluate a measurement system using wave and optical evidence.

Exclusions. Fourier analysis, wave equations by differential calculus, diagnostic interpretation, and detailed imaging reconstruction.

BIO-150 Microorganisms, viruses, and biological evolution — 40 hours#

Prerequisites: BIO-140.

Topic ID Scope and outcome
BIO-151 Compare bacteria, archaea, microbial eukaryotes, and viruses in organization, replication, metabolism, and dependence on hosts.
BIO-152 Explain bacterial growth, horizontal gene transfer, viral cycles, mutation, selection, and the evolution of resistance.
BIO-153 Distinguish sterilization, disinfection, antisepsis, asepsis, and antimicrobial selectivity at principle level.
BIO-154 Use growth curves, plaques, serial dilution, and culture-independent evidence to make bounded quantitative claims.
BIO-155 Explain microbiomes as ecological communities while avoiding simplistic healthy/unhealthy labels and causal overreach.
BIO-156 Apply evolutionary reasoning to host-pathogen interaction, virulence tradeoffs, immune escape, and comparative evidence.

Practice/practical. Aseptic-technique demonstration or supervised practice; safe environmental culture only under approved protocol; serial-dilution simulation; outbreak phylogeny exercise.

Gate. Explain changing population evidence in an antimicrobial-resistance scenario and design a safe discriminating investigation.

Exclusions. Culturing unknown high-risk organisms, pathogen identification for personal health, exhaustive taxonomy, and clinical antimicrobial selection.

PHY-140 Electricity, fields, and circuits — 45 hours#

Prerequisites: PHY-110, CHE-140 recommended.

Topic ID Scope and outcome
PHY-141 Apply charge, Coulomb force, electric field, potential, potential energy, and equipotential reasoning in simple geometries.
PHY-142 Relate current, voltage, resistance, resistivity, power, and energy; solve series/parallel and simple Kirchhoff circuits.
PHY-143 Explain capacitance, dielectric behavior, charging/discharging qualitatively, and membranes as capacitive structures with explicit model limits.
PHY-144 Explain conductivity in metals and ionic solutions and connect electrical measurement to safety and electrode interfaces at survey depth.
PHY-145 Describe magnetic force, fields around currents, induction, and electromagnetic devices at an introductory, algebra-based level.
PHY-146 Identify electrical hazards, grounding, isolation, current paths, and the difference between a measurement model and human exposure.

Practice/practical. Build or simulate series/parallel circuits; determine an unknown resistance; RC trace investigation; electrical-safety case.

Gate. Diagnose a non-working measurement circuit from quantitative evidence and document safe correction.

Exclusions. Maxwell-equation derivations, AC phasors, electrophysiological diagnosis, and device repair beyond supervised low-voltage work.

ORG-210 Organic structure, stereochemistry, and reactivity — 50 hours#

Prerequisites: CHE-140 and molecular portions of BIO-110.

Topic ID Scope and outcome
ORG-211 Interpret line-angle, condensed, wedge-dash, Newman, and skeletal representations; identify constitutional and conformational isomers.
ORG-212 Name and recognize alkanes, alkenes, alkynes, aromatic systems, halides, alcohols, ethers, thiols, amines, aldehydes, ketones, carboxylic acids and derivatives.
ORG-213 Determine formal charge, resonance, aromatic stabilization at survey depth, hybridization, geometry, dipoles, and intermolecular interactions.
ORG-214 Assign stereocentres and R/S, alkene E/Z, enantiomer/diastereomer relationships, meso forms, optical activity, and biological consequences of stereochemistry.
ORG-215 Rank acidity/basicity and nucleophile/electrophile behavior from charge, electronegativity, resonance, induction, orbital, solvent, and steric effects.
ORG-216 Use curved-arrow electron flow, reaction coordinate diagrams, kinetic/thermodynamic control at introductory depth, and equilibrium reasoning.

Practice/practical. Molecular-model portfolio; stereochemical medicine case; acid/base extraction plan; mechanism error correction.

Gate. Infer physical and reactive properties of unfamiliar organic structures and justify each prediction mechanistically.

Exclusions. Comprehensive IUPAC edge cases, pericyclic orbital theory, and memorization of named reactions without mechanism.

PHY-150 Thermal, atomic, nuclear, and radiation physics — 25 hours#

Prerequisites: CHE-130, PHY-130.

Topic ID Scope and outcome
PHY-151 Apply temperature, thermal expansion, heat capacity, phase change, conduction, convection, radiation, and the first law to bounded systems.
PHY-152 Relate photons, spectra, quantized transitions, photoelectric effect, and matter-wave ideas at conceptual/introductory calculation depth.
PHY-153 Explain nuclear composition, binding, isotopes, alpha/beta/gamma processes, half-life, activity, attenuation, and inverse-square behavior.
PHY-154 Distinguish ionizing from non-ionizing radiation, absorbed/equivalent dose concepts, stochastic risk, and basic protection principles.
PHY-155 Compare the physical basis—not clinical interpretation—of radiography, CT, nuclear medicine, ultrasound, and MRI at survey depth.

Practice/practical. Cooling curve or thermal-transfer investigation; half-life simulation; shielding/attenuation dataset; modality comparison.

Gate. Calculate and communicate a radiation/thermal exposure scenario with assumptions, units, uncertainty, and risk-language discipline.

Exclusions. Quantum derivations, radiation treatment planning, image diagnosis, and operation of regulated radiation sources.

ORG-220 Organic reaction families and biological mechanisms — 60 hours#

Prerequisites: ORG-210.

Topic ID Scope and outcome
ORG-221 Compare substitution and elimination (SN1, SN2, E1, E2) by substrate, nucleophile/base, solvent, stereochemical, kinetic, and product evidence.
ORG-222 Explain electrophilic addition to alkenes/alkynes, hydration, oxidation/reduction, and regio-/stereochemical outcomes at introductory depth.
ORG-223 Explain nucleophilic addition to carbonyls and relate aldehyde/ketone chemistry to biological molecules.
ORG-224 Explain nucleophilic acyl substitution and compare carboxylic-acid derivatives, hydrolysis, condensation, and biological acyl transfer.
ORG-225 Explain alcohol, amine, thiol, phosphate, and redox transformations relevant to biomolecules.
ORG-226 Plan short reaction sequences from a supplied reaction set, tracking chemoselectivity, stereochemistry, yield, purification, and hazards.

Practice/practical. Safe esterification or hydrolysis; reaction-mechanism studio; product-distribution dataset; green-chemistry comparison.

Gate. Predict products and mechanisms in an unfamiliar but bounded network, then select evidence that distinguishes alternatives.

Exclusions. Unbounded multistep synthesis, organometallic breadth beyond selected examples, and advanced synthesis strategy.

BCH-210 Amino acids, proteins, and enzymes — 55 hours#

Prerequisites: BIO-120, CHE-140, ORG-210.

Topic ID Scope and outcome
BCH-211 Draw amino-acid charge states, estimate predominant form from pH/pKa, classify side-chain chemistry, and calculate peptide net charge in bounded cases.
BCH-212 Explain peptide-bond properties and primary through quaternary structure, folding forces, disorder, chaperones, denaturation, and aggregation.
BCH-213 Relate structure to binding, cooperativity, allostery, and the oxygen-binding behavior of myoglobin/haemoglobin as models.
BCH-214 Apply Michaelis-Menten concepts, Km, Vmax, turnover, catalytic efficiency, and common inhibition patterns to data without overinterpreting simplified kinetics.
BCH-215 Explain catalytic strategies, cofactors/coenzymes, zymogens, covalent and allosteric regulation, and feedback.
BCH-216 Select chromatography, electrophoresis, centrifugation, immunodetection, activity assay, and mass-spectrometry evidence by question and limitation.

Practice/practical. Protein standard curve and unknown; enzyme kinetics/inhibition; chromatography or electrophoresis simulation/physical lab; haemoglobin curve case.

Gate. Infer protein function and regulation from sequence/structure, purification, binding, and kinetic evidence.

Exclusions. Structural determination pipelines, enzyme mechanism catalogues, and clinical protein-disease management.

ORG-230 Separation, spectroscopy, and structure evidence — 40 hours#

Prerequisites: ORG-220, optics portions of PHY-130.

Topic ID Scope and outcome
ORG-231 Select extraction, recrystallization, distillation, filtration, and chromatography from physical-property reasoning.
ORG-232 Interpret TLC and introductory column/GC/HPLC outputs, retention, resolution, standards, and purity limitations.
ORG-233 Interpret characteristic IR absorptions and connect vibrations to functional groups.
ORG-234 Interpret introductory proton NMR chemical shift, integration, splitting, equivalence, and exchange using provided ranges.
ORG-235 Interpret molecular ion, fragments at survey depth, isotope patterns, and accurate-mass/formula evidence in mass spectra.
ORG-236 Integrate formula, reactivity, separation, IR, NMR, and MS evidence to discriminate plausible structures.

Practice/practical. Pigment or analgesic chromatography; virtual spectra; extraction/purification design; blind structure-elucidation set.

Gate. Produce an auditable structure argument from a multi-technique evidence packet.

Exclusions. Carbon NMR depth, multidimensional NMR, spectral prediction algorithms, and instrument maintenance.

BCH-220 Carbohydrates, lipids, membranes, and nucleotides — 45 hours#

Prerequisites: BCH-210, ORG-220.

Topic ID Scope and outcome
BCH-221 Relate monosaccharide stereochemistry, ring formation, glycosidic bonds, storage/structural polysaccharides, and glycoconjugates to function.
BCH-222 Compare fatty acids, triacylglycerols, phospholipids, sphingolipids, steroids, eicosanoids at survey depth, and their physical/biological roles.
BCH-223 Explain membrane asymmetry, fluidity, curvature, rafts as a qualified model, transport proteins, gradients, and membrane potential foundations.
BCH-224 Explain nucleotide chemistry, phosphodiester bonds, base pairing, nucleic-acid stability, ATP/GTP roles, and selected nucleotide-derived cofactors/signals.
BCH-225 Connect chemical structure to digestion, transport, storage, signalling, and experimentally observable behavior without turning nutrient chemistry into diet advice.

Practice/practical. Lipid-membrane model; carbohydrate stereochemistry; partitioning/chromatography dataset; nutrition-claim evidence audit.

Gate. Explain a membrane transport and storage problem from molecular structures through system consequences.

Exclusions. Personalized nutrition advice, complete lipidomics, and specialized glycobiology.

BCH-230 Bioenergetics and central metabolism — 60 hours#

Prerequisites: BCH-210, BCH-220, CHE-140.

Topic ID Scope and outcome
BCH-231 Relate free energy, equilibrium, mass action, coupling, phosphorylation potential, redox carriers, and compartmentation.
BCH-232 Trace glycolysis and gluconeogenesis by carbon, energy, redox, irreversible control points, reciprocal regulation, and tissue context at first-semester depth.
BCH-233 Explain glycogen synthesis/breakdown and the pentose-phosphate pathway by purpose, regulation, and products.
BCH-234 Trace pyruvate dehydrogenase, citric-acid cycle, anaplerosis/cataplerosis at survey depth, and their regulation.
BCH-235 Explain electron transport, proton-motive force, ATP synthase, oxidative phosphorylation, uncoupling, reactive oxygen species, and inhibitor evidence.
BCH-236 Trace fatty-acid mobilization, transport, beta-oxidation, synthesis, and ketone-body production/use at first-semester depth.
BCH-237 Explain amino-acid carbon/nitrogen handling at overview depth; the urea cycle is enrichment, not an MCAT-derived core claim.
BCH-238 Compare aerobic/anaerobic yields using clearly declared conventions and reconcile fed, fasting, exercise, and selected organ-context signals.

Practice/practical. Respirometry or simulation; pathway perturbation maps; comparative ATP accounting; multi-tissue fasting case.

Gate. Trace labelled atoms and energy/redox consequences through an unfamiliar metabolic perturbation and predict discriminating measurements.

Exclusions. Memorizing every enzyme structure, exhaustive inborn errors, urea-cycle detail as a common-core requirement, and treatment planning.

BCH-240 Integrated information flow and biochemical regulation — 40 hours#

Prerequisites: BIO-140, BCH-230.

Topic ID Scope and outcome
BCH-241 Integrate DNA replication, transcription, translation, turnover, compartmentation, and post-translational modification in a regulated system.
BCH-242 Explain receptor binding, second messengers, phosphorylation, gene regulation, amplification, feedback, and desensitization across time scales.
BCH-243 Interpret omics-style heat maps, fold change, normalization, replicates, multiple-testing caution, and pathway enrichment only at conceptual depth.
BCH-244 Connect molecular perturbations to cellular phenotype while separating loss of function, gain of function, dominant-negative, compensation, and correlation.
BCH-245 Select molecular and biochemical assays that jointly test a mechanism and specify positive, negative, loading, and process controls.

Practice/practical. Integrated signalling dataset; blot/assay control audit; gene-to-metabolite causal diagram; research-figure journal club.

Gate. Defend a causal molecular mechanism using a multi-panel dataset and propose the most informative next experiment.

Exclusions. Independent analysis of patient omics, advanced causal inference, and drug-selection recommendations.

10. Medicine-facing bridge#

These modules are required for the EmbeddedKnowledge Premed completion because they make the foundational sciences usable at the threshold of medical study. The source adjudication does not establish them all as universal entrant requirements. They are marked EK-BRIDGE in the knowledge graph and on learner records.

MED-310 Human structure, transport, and homeostasis — 75 hours#

Prerequisites: all 100-level Biology; PHY-120; BCH-220.
Scope rule: structure-function and homeostatic reasoning, not clinical diagnosis or memorization of exhaustive anatomical detail.

Topic ID Scope and outcome
MED-311 Organization and tissues: orient anatomical planes/terms; compare epithelial, connective, muscle, and nervous tissue; infer function from microstructure.
MED-312 Homeostasis: construct negative/positive feedback models; distinguish regulated variable, sensor, integrator, effector, set range, compensation, and failure.
MED-313 Nervous system: relate membrane potentials, synapses, neurotransmission, sensory/motor organization, autonomic control, and neural integration at introductory depth.
MED-314 Endocrine system: compare peptide/steroid signalling, axes, feedback, receptor regulation, and time course.
MED-315 Musculoskeletal system: connect bone, joint, muscle microstructure, excitation-contraction coupling, force-length/velocity ideas, levers, and repair at survey depth.
MED-316 Cardiovascular system: trace circulation; relate cardiac cycle, electrical conduction, pressure-flow-resistance, vessels, exchange, and regulation.
MED-317 Respiratory system: relate ventilation, compliance, diffusion, perfusion, haemoglobin transport, acid-base contribution, and control of breathing.
MED-318 Renal and fluid balance: trace filtration, reabsorption, secretion, concentration/dilution, electrolytes, osmolarity, volume, and acid-base regulation at introductory depth.

Practice/practical. Histology image atlas; feedback-loop perturbations; ECG principles simulation (not interpretation for care); spirometry demonstration/data; pressure-flow model; urinalysis simulation with privacy-safe synthetic data.

Gate. Explain a multi-system homeostatic perturbation from molecular transport through feedback, identifying observations that the model does and does not explain.

Exclusions. Named-disease catalogues, diagnostic thresholds, physical examination credentialing, treatment, and patient-specific inference.

MED-320 Digestion, reproduction, development, and integrated physiology — 45 hours#

Prerequisites: MED-310, BCH-230.

Topic ID Scope and outcome
MED-321 Digestive system: trace motility, secretion, digestion, absorption, portal transport, liver/pancreas roles, and regulation by structure and molecular process.
MED-322 Energy balance: distinguish energy intake/expenditure, storage/mobilization, hormonal signals, and population association from individual causation.
MED-323 Reproductive systems: explain gametogenesis, endocrine cycles, fertilization, and reproductive anatomy at introductory, inclusive depth.
MED-324 Development: trace cleavage, implantation, germ layers, morphogenetic patterning at survey depth, placental exchange, and major developmental principles.
MED-325 Exercise and environmental integration: integrate cardiovascular, respiratory, neural, muscular, renal, endocrine, and metabolic responses over time.
MED-326 Life-course physiology: distinguish growth, maturation, ageing, reserve, adaptation, and pathological claims with appropriate uncertainty.

Practice/practical. Digestion/absorption model; endocrine-cycle data; development concept map; exercise-response investigation with opt-out/equivalent dataset.

Gate. Construct and defend a time-resolved, cross-system model of feeding, fasting, exercise, pregnancy, or thermal stress from an unseen evidence set.

Exclusions. Fertility advice, obstetric management, diet prescription, developmental diagnosis, and detailed embryological anatomy.

MED-330 Immunity, infection, biotechnology, and public responsibility — 50 hours#

Prerequisites: BIO-150, BCH-240; MED-310 may be concurrent.

Topic ID Scope and outcome
MED-331 Distinguish barriers, innate sensing, inflammation, complement, phagocytes, antigen presentation, and the logic of rapid defence.
MED-332 Explain B/T lymphocyte development at survey depth, clonal selection, antibodies, cell-mediated responses, tolerance, contraction, and memory.
MED-333 Compare active/passive and natural/artificial immunity and explain vaccination using individual and population evidence without making personal recommendations.
MED-334 Explain infection as an interaction among agent, host, environment, transmission, virulence, dose, immunity, and time—not as a property of a microbe alone.
MED-335 Explain hypersensitivity, autoimmunity, immune deficiency, transplant rejection, and immune evasion as mechanism classes at survey depth.
MED-336 Evaluate diagnostic-assay concepts using sensitivity, specificity, likelihood information at introductory depth, predictive value, reference standards, and spectrum bias.
MED-337 Evaluate PCR, sequencing, CRISPR, recombinant products, immunoassays, cell technologies, and antimicrobial interventions by mechanism, evidence, uncertainty, access, dual-use, and ethical limits.
MED-338 Apply biosafety, data privacy, informed consent, community impact, antimicrobial stewardship principles, and responsible public communication to a bounded scenario.

Practice/practical. Immunoassay simulation; outbreak model; vaccine-evidence appraisal; diagnostic-test natural frequencies; biotechnology ethics deliberation.

Gate. Respond to an evolving infectious/immune evidence packet: explain mechanisms, calculate test implications, critique a study, and produce a public-facing correction that stays outside medical advice.

Exclusions. Diagnosis, vaccination or antimicrobial advice, culturing pathogens, advanced immunophenotyping, and clinical immunology management.

11. Integration and capstone#

INT-300 Longitudinal integration studios — 30 hours accounted separately#

Integration studios occur at six transition points; they do not wait until the end.

Studio ID Trigger Integrative problem Required artefact
INT-301 after first 100-level cluster Membrane transport and solution chemistry annotated model + calculation audit
INT-302 after CHE-140/BIO-140 Enzyme, pH, gene regulation, and experimental controls multi-panel evidence explanation
INT-303 after Physics core Pressure, flow, gas exchange, optics, and measurement model comparison + uncertainty memo
INT-304 after Organic/Biochem core Molecular structure to metabolism atom/energy trace + mechanism defence
INT-305 during Medicine bridge Multi-system homeostasis over time causal graph + narrated explanation
INT-306 before capstone Behaviour, society, biology, and ethical evidence (uses pathway material or supplied primer) stakeholder/evidence brief

At least four studios must reach T (transfer) and the remainder M. An integrative answer earns no credit for naming many facts without specifying causal or evidential relationships.

CAP-400 Premed readiness capstone — 30 hours#

Prerequisites: all common-core and bridge gates at M; pathway substantially complete.

Learners choose an unfamiliar, non-diagnostic problem from an approved bank or propose one. Examples include oxygen delivery at altitude, antibiotic resistance in a community, an enzyme variant and metabolism, optical screening technology, or stress and health inequality. Personal medical cases are not accepted.

Required products:

  1. CAP-401 a one-page question, scope, assumptions, safety/ethics, and evidence plan;
  2. CAP-402 a reproducible analysis package containing source ledger, data dictionary, calculations, figures, and change log;
  3. CAP-403 a 2,500–3,500 word synthesis connecting at least four domains and evaluating at least one primary study;
  4. CAP-404 an 8–10 minute public explanation or accessible equivalent;
  5. CAP-405 a 20-minute oral defence or text-based synchronous defence with two assessors where feasible;
  6. CAP-406 a post-defence correction memo identifying what changed and why.

The capstone cannot compensate for missing module outcomes. Its purpose is transfer, synthesis, provenance, and intellectual honesty.

12. Route and breadth pathways#

Every learner completes at least one pathway. Pathways are additions to the portable core, not claims about universal preparation. Institution-facing pathways require annual review because admissions rules change.

Instrumentation limitation (curriculum version 1.1). Only PW-US, PW-BIO and PW-QNT are instrumented in the v1 knowledge graph (site/data/premed-graph.json) as trackable atomic outcomes. PW-UK and PW-ES are documented routes that are NOT yet instrumented. Their route-defining outcomes — UCAT familiarization (UK-240), the QAA Access baseline (UK-230), the Spanish admission audit (ES-211), and the open-response studio (ES-250) — are not among the graph's 388 atomic outcomes, so a learner cannot currently satisfy the section 6.2 "one completed route/pathway" requirement through PW-UK or PW-ES, and contributors cannot yet author lessons against those outcomes. Learners on those routes should complete PW-US, PW-BIO or PW-QNT for the completion requirement and treat the UK/Spain material below as an uninstrumented reading and audit guide. Instrumenting both routes is planned for a later curriculum version.

PW-US United States graduate-entry / MCAT — 200 hours#

Status: route-specific, not global core. Always verify each target school's current coursework and laboratory policy.

Module Topic-level outcomes
PSY-211 Mind and behaviour Explain biological bases of behaviour, sensation/perception, consciousness, learning, memory, language, cognition, motivation, emotion, stress, development, personality, psychological disorder concepts, and treatment-evidence categories at first-semester depth.
SOC-221 Social structure and health Explain socialization, interaction, groups, organizations, institutions, culture, deviance, demographics, migration, urbanization, stratification, inequality, race/ethnicity as social processes, gender, age, and social determinants using non-essentialist language.
BHV-230 Person in context Integrate attitudes, attribution, identity, self, prejudice, conformity, social support/capital, access, environment, behaviour change, and biopsychosocial evidence.
CAR-240 Critical analysis Identify argument structure, assumptions, tone, evidence, analogy, contradiction, author perspective, and implications in humanities/social-science passages without relying on outside content.
MCAT-250 Format transfer Apply common-core knowledge under representative passage/data conditions; build timing only after untimed accuracy; use official-style practice to locate—not conceal—node gaps.

Route outcome PLO-US. Solve integrated MCAT-level science and behavioural passages at the AAMC-stated introductory depths and create an institution-specific prerequisite audit. EmbeddedKnowledge does not promise a score.

Route gate. Three spaced, mixed-form readiness sets plus an oral error analysis. Official AAMC materials should be used under their terms, not reproduced into the course.

PW-UK UK direct-entry / Access to HE orientation — 180 hours#

Status: route-specific and institution-dependent. The UCAT is an aptitude test rather than a science syllabus. Not instrumented in curriculum version 1.1: no module of the v1 knowledge graph maps to PW-UK, and none of the outcomes below exist as trackable atomic outcomes, so this route cannot yet satisfy the section 6.2 pathway requirement and cannot yet be authored against. Planned for a later curriculum version.

Module Topic-level outcomes
UK-211 Qualification audit Map target-course A-level/IB/Access subject and grade rules from current primary admissions pages; identify gaps without treating sector summaries as final authority.
UK-220 Scientific practical portfolio Demonstrate planning, safe implementation, observation, quantitative treatment, evaluation, and independent reporting across biology and chemistry; where relevant, align evidence to common practical-assessment concepts.
UK-230 Access to HE medicine baseline Demonstrate the QAA descriptor's breadth: chemistry and biology/human biology, an additional science/mathematics component, numerical data, study skills, and professional behaviours.
UK-240 Aptitude familiarization Practise current UCAT verbal, decision, quantitative, and situational-judgement constructs using authorized materials; do not invent science content for UCAT.
UK-250 Constructed scientific communication Complete open-response explanation, practical/research/statistical report, oral presentation, reflective work, and representative selected-response tasks.

The QAA Access to HE Diploma Subject Descriptor for Medicine is an important access baseline, not a substitute qualification here. The actual diploma has 60 credits: 45 graded Level 3 credits, including at least 15 Chemistry, 15 Biology/Human Biology, and 9 other science/mathematics; its ungraded Level 3 minimum includes 3 credits each in numerical data, study skills, and professional behaviours. EmbeddedKnowledge mirrors the outcomes—atoms, bonds, formulae, periodicity, moles, acids/bases, rates/equilibria, enthalpy, organic chemistry, cells, biomolecules, gene expression, heredity, cardiovascular/respiratory/digestive and further systems, plus laboratory design/performance/interpretation—and its assessment mix spans unseen work, selected response, essays, practical/research/statistical reports, oral presentation, and reflection. The gates remain retakeable. EmbeddedKnowledge does not award QAA credit.

Route outcome PLO-UK. Produce a current application requirement map and a QAA-informed portfolio spanning scientific knowledge, practical work, data, study, communication, and professional behaviour.

PW-ES Spain / continental direct-entry orientation — 180 hours#

Status: route-specific. PAU rules and university weighting tables must be versioned by year and jurisdiction. Not instrumented in curriculum version 1.1: no module of the v1 knowledge graph maps to PW-ES, and none of the outcomes below exist as trackable atomic outcomes, so this route cannot yet satisfy the section 6.2 pathway requirement and cannot yet be authored against. (The graph's spain-bach-pau filter tag marks Spanish-curriculum content inside other modules; it is not the same thing as an instrumented PW-ES route.) Planned for a later curriculum version.

Module Topic-level outcomes
ES-211 Admission audit Distinguish the national PAU access formula and obligatory exercises from university/regional subject weightings; build a current, source-linked target table.
ES-220 Biology emphasis Consolidate biomolecules, molecular genetics, cell biology, metabolism including autotrophic anabolism (photosynthesis and chemosynthesis), biotechnology, and immunity; distinguish second-year national minimum from broader biology. RD 243/2022 specifies autotrophic anabolic pathways, so photosynthesis belongs to this route; it contains no ecology block and no broad plant-anatomy unit.
ES-230 Chemistry/physics/math emphasis Solve open and semi-constructed problems at the selected jurisdiction's current specification depth and explain reasoning in the required assessment language.
ES-240 Metabolism and biotechnology depth Quantitatively compare glycolysis, fermentation, beta-oxidation, citric-acid cycle, electron transport, oxidative phosphorylation; explain PCR, restriction methods, cloning, and CRISPR.
ES-250 Open-response studio Construct a defensible response, expose intermediate reasoning, interpret novel evidence, and self-audit against published criteria.

Route outcome PLO-ES. Demonstrate the selected specification outcomes and maintain a versioned PAU/university-weighting audit without presenting one university's table as a national rule.

PW-BIO Broad biological literacy — 120 hours#

For learners targeting AP/A-level/IB/Abitur/Baccalaureat breadth or a later bioscience degree. This pathway includes topics important to biology but weak as a universal premedical minimum.

Module Topic-level outcomes
ECO-211 Ecology Model populations, communities, competition, predation, succession, biodiversity, nutrient cycles, energy flow, and anthropogenic change; analyze field evidence.
PLT-220 Plant biology Explain plant form, meristems, transport, mineral nutrition, hormones/tropisms, reproduction, and adaptation.
PLT-230 Photosynthesis Explain light capture, electron transport, chemiosmosis, carbon fixation, photorespiration, and environmental response, linked to but not mislabeled as MCAT content.
EVO-240 Evolutionary breadth Extend population genetics to phylogenetics, evo-devo survey, coevolution, and macroevolutionary evidence.
BIO-250 Field/practical inquiry Design and report an ethical observational or manipulative ecology/plant investigation with sampling and statistical reasoning.

Route outcome PLO-BIO. Explain and investigate biological systems beyond medicine while clearly distinguishing this breadth from MCAT requirements.

PW-QNT Calculus and extended quantitative science — 160 hours#

For mathematics-rich national routes, quantitative bioscience, physics preparation, or learner interest. Calculus is explicitly outside the MCAT mathematics specification and is not a portable entrant minimum.

Module Topic-level outcomes
QNT-211 Calculus Interpret limits, derivatives, and integrals; solve basic optimization, rate, accumulation, and separable growth/decay problems.
QNT-220 Vectors and multivariable ideas Work with vector components, dot products, partial-change intuition, gradients at survey depth, and parameter sensitivity.
QNT-230 Differential models Analyze simple exponential/logistic, compartment, oscillatory, and pharmacokinetic teaching models without clinical dosing use.
QNT-240 Extended inference Use simulation, resampling, multiple-comparison awareness, simple multivariable models, and reproducible code or spreadsheet workflows.
QNT-250 Quantitative project Build, validate, and communicate one model using a public or synthetic biological dataset.

Route outcome PLO-QNT. Use calculus, simulation, and extended statistics to construct and criticize a biological model.

Custom institution pathway PW-CUS#

A learner may propose a 120–240 hour pathway mapped to a named, current primary-source specification. Approval requires: stable topic IDs, source versions, measurable outcomes, no collision with the common-core claims, comparable evidence volume, and a route gate. This mechanism supports IB HL, particular A-level boards, Abitur Länder, French specialties, India/NEET, GAMSAT, or an individual school's prerequisites without pretending they are interchangeable.

13. Practical and laboratory curriculum#

13.1 Principle and notation#

Practical work has three valid but non-equivalent modalities:

  • P physical: learner handles equipment/materials under an approved risk assessment;
  • S simulation: learner makes experimental choices in a model and analyzes generated data;
  • D dataset/observation: learner analyzes documented real-world or recorded experimental evidence.

The transcript reports the modality for every investigation. A simulation may satisfy design and analysis outcomes but never certifies pipetting, microscopy setup, aseptic handling, dissection, electrical construction, chemical handling, or other physical skill. External programs may reject all remote practical evidence.

13.2 Required investigation families#

Complete at least twelve, including one from every row. For the blended-practical notation, at least four must be physical, at least one each in Biology and Chemistry, under qualified local supervision where risk requires it.

Lab ID Investigation family Minimum assessable evidence Permitted modality
LAB-01 Measurement, calibration, density instrument choice, calibration, repeated measures, uncertainty P/S/D
LAB-02 Solution preparation and reaction quantity preparation record, stoichiometry, yield, waste/safety P/S
LAB-03 Calorimetry or thermal transfer energy model, controls, loss analysis P/S/D
LAB-04 Kinetics or equilibrium variable manipulation, rate/equilibrium distinction, graph/model P/S/D
LAB-05 Acid-base titration/buffer standardization or calibration, curve, equivalence, uncertainty P/S/D
LAB-06 Membranes/osmosis biological material/model, controls, quantitative response P/S/D
LAB-07 Microscopy/image analysis scale, sampling, artifact, reproducible measurement P/S/D
LAB-08 Enzyme activity initial-rate logic, replicates, environmental/inhibitor effect P/S/D
LAB-09 Genetics/molecular method cross or PCR/electrophoresis evidence, controls, inference P/S/D
LAB-10 Motion/force/energy measurement model, graph, conservation or force analysis P/S/D
LAB-11 Fluid/circuit/wave/optics model prediction, safe apparatus, parameter estimate P/S/D
LAB-12 Separation/spectroscopy method selection, standards, evidence-based identification P/S/D
LAB-13 Physiology consent/opt-out, non-diagnostic measurement, variation, privacy P/S/D
LAB-14 Independent inquiry question, preregistered plan, risk review, data, revision, limitations P/S/D

13.3 Practical report standard#

Each investigation record contains: question and rationale; method and deviations; hazard/ethics check; raw data with units and provenance; transformations/formulas; visualizations; uncertainty; results; interpretation; alternatives and limitations; reproducibility package; and a correction log. Stock “method/results/conclusion” prose without raw evidence is insufficient.

13.4 Safety limits#

At-home work is limited to an approved low-risk list. It excludes regulated radiation sources, mains electricity construction, unknown human samples, blood/body fluids, vertebrate dissection, culturing unknown or potentially pathogenic organisms, prescription/controlled substances, unsupervised corrosive/flammable/toxic reagents, self-experimentation that changes medication/diet/sleep, and any experiment presented as personal medical testing. A learner can always choose a simulation or supplied dataset without penalty.

14. Learning design and weekly experience#

Every standard study week uses a common cycle. Learners may change media, but not the outcome or evidence standard.

  1. Orient (30–45 min): inspect the node map, prerequisite check, why-it-matters case, and explicit exclusions.
  2. Acquire (4–7 h): read, watch, or listen to source-linked explanations; complete worked-example pauses and representation checks.
  3. Retrieve (1–2 h): spaced short-answer and recognition prompts selected by node state, including earlier domains.
  4. Model and solve (4–6 h): quantitative problems, diagrams, mechanisms, graph reading, and explanation comparison.
  5. Investigate (2–4 h average): practical, simulation, dataset, or research-method studio.
  6. Discuss (1 h): AI Socratic dialogue and, where available, peer/tutorial discussion. The learner submits the conversation's correction note, not a transcript dump.
  7. Apply (2–3 h): medicine-facing or society-facing case that requires transfer but no personal medical advice.
  8. Reflect and plan (30 min): classify errors, compare confidence with performance, schedule remediation and delayed retrieval.

Required recurring activities#

  • one cumulative mixed set every week;
  • one graph/table/figure interpretation every week;
  • one substantive explanation from memory every week;
  • one primary-source figure or method excerpt every two weeks after QRS-111;
  • one integration studio at each curricular transition;
  • one source/provenance and accessibility audit each term;
  • one protected recovery week after every 10–12 teaching weeks.

The system must offer a “minimum viable study day” of 15–25 minutes—one retrieval set, one worked example, and the next explicit action—so a disrupted week does not become abandonment.

15. Assessment system#

15.1 Evidence categories#

The course reports mastery outcomes, but the following conventional weighting is retained for audit and for learners who need a familiar summary. No category can compensate for an unmastered required node.

Category Audit weight Typical evidence
Spaced retrieval and calibration 10% delayed checks, confidence accuracy, correction quality
Quantitative/problem-solving portfolio 15% mixed sets, complete units, model assumptions, alternative strategies
Scientific reasoning and source appraisal 15% design critiques, paper analyses, causal/evidence judgments
Practical/investigation portfolio 20% twelve investigations and reproducibility audits
Module mastery gates 20% retakeable unseen tasks, oral/written explanation, transfer item
Integration studios 10% cross-domain causal models and evidence briefs
Capstone and defence 10% synthesis, reproducibility, public explanation, correction memo

15.2 Assessment layers#

  1. Checks: 2–10 minute, low stakes, immediate explanatory feedback. Unlimited attempts; later attempts vary the surface form.
  2. Practice sets: untimed by default, hints fade, answer explanations require error classification. Practice completion never proves mastery by itself.
  3. Socratic probes: tutor asks for prediction, mechanism, evidence, boundary case, and self-correction. A human-auditable summary is stored.
  4. Performances: practicals, data analyses, paper critiques, models, and explanations scored with analytic rubrics.
  5. Mastery gates: unseen, bounded, retakeable only after a targeted prescription; forms are equivalent by blueprint rather than repeated.
  6. Retention checks: short delayed probes at 7–14 days and at least 21 days; downstream tasks can also supply retention evidence.
  7. Capstone: integrated transfer with defence and revision.

15.3 Gate blueprint#

Every disciplinary gate samples:

  • 20–30% accurate explanation and retrieval;
  • 25–35% quantitative, symbolic, or representational reasoning;
  • 20–30% novel data or experimental-design reasoning;
  • 15–25% transfer to a medicine-facing or authentic scientific context;
  • at least one limitation/uncertainty item and one misconception trap.

Gate forms are untimed unless a route explicitly requires pacing practice. The normal pass rule is ≥80% overall, ≥70% in every sampled dimension, and 100% on named safety/integrity items. Oral verification is used when authorship or conceptual ownership is unclear, never as punishment.

15.4 Common analytic rubric (4 levels)#

Dimension 4 — Transfer 3 — Mastery 2 — Developing 1 — Insufficient
Accuracy and scope Accurate, appropriately qualified, connects boundaries Accurate on required scope; no material misconception Mostly accurate but omission or imprecision changes part of conclusion Major misconception, contradiction, or unsafe claim
Mechanistic reasoning Coherent multilevel causal chain; tests alternatives Correct causal/mechanistic chain with relevant steps Names factors but leaves causal gaps or confuses levels Restates outcome, uses teleology, or asserts causation without mechanism/evidence
Quantitative work Correct model, units, uncertainty, sensitivity, plausibility Correct setup/calculation/units and interpretation Minor procedural errors or weak interpretation Wrong model/denominator/units or uninterpretable result
Evidence and design Triangulates evidence; identifies bias and decisive follow-up Interprets data and controls; states warranted conclusion/limits Partial interpretation or generic limitations Ignores controls, confounds, or overclaims
Representation Moves consistently among words, equations, graphs, diagrams Uses the requested representation correctly Understandable but incomplete/inconsistent Representation conflicts with claim or hides reasoning
Communication and provenance Audience-fit, concise, accessible, fully traceable Clear, organized, sources/tool use disclosed Meaning recoverable; citation/accessibility gaps Misleading, copied, inaccessible, or source provenance absent
Reflection and correction Diagnoses root cause, generalizes repair, verifies it Corrects error and states prevention strategy Corrects answer without explaining cause Defends error, edits invisibly, or cannot reproduce work

A score of 3 on all dimensions required by the task constitutes mastery. A 4 is evidence of transfer, not extra decorative detail.

15.5 Practical rubric additions#

Practical work also requires a 3 or 4 in: safety/ethics; method fitness; raw-record quality; calibration/controls; data treatment; uncertainty/limitations; reproducibility. A serious safety breach ends the procedure safely and moves the learner to remediation; it does not permanently bar a retry.

15.6 Capstone rubric#

The capstone uses the common rubric plus four weighted dimensions:

Dimension Weight Mastery anchor
Cross-domain integration 25% at least four domains linked by explicit, correct relationships rather than juxtaposed sections
Evidence and reproducibility 25% source/data provenance, auditable analysis, result reproduced by assessor
Scientific judgment 20% assumptions, alternatives, uncertainty, ethics, and boundary of claim are material to conclusion
Communication and defence 20% expert paper and public artefact are accurate; answers reveal ownership and allow correction
Revision 10% correction memo makes substantive, traceable changes after critique

Acceptance requires ≥3/4 on each dimension. Learners revise and defend again when needed.

15.7 Record issued#

The public/exportable record states:

  • curriculum and source-alignment version;
  • each module and outcome state (M, R, or T only; earlier states remain private by default);
  • dates of first mastery and most recent retention evidence;
  • practical titles and modality (P, S, D), never implying hands-on work where none occurred;
  • pathway(s) and capstone title;
  • accommodations used only when the learner elects disclosure;
  • an explicit non-credit/non-licensure notice.

16. Accessibility, inclusion, and learner safety#

The course follows an accommodation-by-design principle:

  • all essential video has captions and a transcript; audio has a text equivalent;
  • diagrams include alt text and a structured description; color is never the only code;
  • math is supplied in accessible notation plus a plain-language reading;
  • interactions are keyboard-operable; timed animation can pause; flashing content is excluded;
  • PDFs are not the sole presentation of required material where a structured HTML alternative can be provided;
  • learners can replace speaking/listening performances with live text or equivalent modes while preserving the reasoning outcome;
  • extended time is unnecessary for untimed gates; scheduled defences allow rest breaks and flexible time zones;
  • practicals have non-penalizing simulation/data alternatives for disability, location, cost, pregnancy, allergy, religious/ethical concerns, or simple preference;
  • physiology activities never require disclosure of health information, sex characteristics, disability, weight, medication, or diagnosis;
  • examples use diverse bodies and populations without presenting a demographic average as a biological norm;
  • sex, gender, race, ancestry, disability, and socioeconomic position are represented with scientifically appropriate constructs and explicit limits;
  • distressing topics carry advance notices and equivalent cases where possible.

Accessibility changes the path, medium, or timing—not the scientific outcome being demonstrated. When an outcome genuinely depends on a physical action, the record accurately marks whether that action was performed.

17. Academic integrity, AI, and privacy#

17.1 Integrity standard#

Learners may collaborate, consult sources, and use tools on learning tasks unless a gate is marked closed-resource. They must preserve authorship and provenance. Prohibited conduct includes fabricated data or citations, undisclosed copying, submitting another person's reasoning, changing raw data without a log, using personal health data without approval, or having an AI generate evidence the learner cannot explain and defend.

17.2 AI use#

AI is permitted for questioning, alternative explanations, feedback, language support, code/spreadsheet debugging, and formative generation when:

  • the learner discloses tool/model and material use in assessed work;
  • all factual and bibliographic claims are checked against accessible sources;
  • no confidential, personal-health, or third-party data are uploaded;
  • the learner retains drafts, prompts or an equivalent use log when AI materially shaped the work;
  • the learner can reproduce calculations and defend conclusions without the tool.

AI output is never a source solely because it is fluent. Mastery gates may require controlled conditions and a brief authorship verification.

17.3 Citation and licenses#

Use a consistent citation system (APA, Vancouver, or a discipline-appropriate equivalent). Cite exact edition/version and retrieval date for mutable web sources. Open licenses are asset-specific: provider names such as “OpenStax” or “LibreTexts” do not establish one blanket license. Before adapting content, record title, edition, URL/format, displayed license, attribution text, modification, retrieval date, and intended use in the rights ledger.

18. Mastery recovery and remediation#

18.1 Error taxonomy#

Every substantive miss is classified as one or more of:

  • RCL retrieval gap;
  • VOC terminology/reading gap;
  • REP representation translation gap;
  • MOD wrong or misapplied model;
  • QNT algebra/unit/denominator/numeracy gap;
  • MEC causal/mechanistic gap;
  • EVD data/design/evidence gap;
  • PRE missing prerequisite;
  • CAL confidence-calibration problem;
  • SAF safety, ethics, privacy, or scope problem.

18.2 Recovery protocol#

  1. Stop and name the failing node and error class.
  2. Check prerequisite nodes; reopen the earliest insecure dependency, not the whole module.
  3. Complete a contrasting example and explain why the original strategy failed.
  4. Produce a fresh representation from memory.
  5. Solve two varied problems without hints, separated in time.
  6. Retry an equivalent gate no earlier than the prescribed interval (normally 24 hours; longer for repeated high-confidence misconceptions).
  7. Schedule delayed retention evidence.

After two unsuccessful gate attempts, a tutor or structured diagnostic reviews the prerequisite map. After three, the learner receives a rewritten route through the node, an alternate modality, and a live/human review where available. The standard does not fall; the route changes.

18.3 Lapse policy#

A later failure does not erase historical evidence. A mastered node moves to “review due,” and high-risk downstream work is paused only if the lapse is material. One successful bounded refresh restores active mastery; recurrent lapses trigger a broader prerequisite audit.

18.4 Motivation protection#

Progress views show secure nodes, next reachable nodes, hours invested, and recovered misconceptions—not rank, streak shame, or peer comparison. A learner can declare a recovery week, reduce to the minimum viable study day, or switch media without resetting progress. Inactivity triggers a compassionate re-entry diagnostic, not a backlog dump.

19. Suggested schedules and workload#

19.1 Standard 72-week route (22–24 hours/week)#

Block Weeks Main modules Milestone
Welcome Before week 1 WEL-000 understand the journey and destination
Placement/on-ramp 0–6 as needed diagnostics, ONR-000 individualized starting map
A. Scientific inquiry and language 1–8 QRS-100, CHE-110, BIO-110 INT-301
B. Particles to cells 9–16 CHE-120, BIO-120, PHY-110 first practical review
C. Matter, inheritance, transport 17–24 CHE-130, BIO-130, PHY-120 cumulative gate + recovery week
D. Regulation and measurement 25–32 CHE-140, BIO-140, PHY-130 INT-302/INT-303
E. Reactivity and systems 33–40 BIO-150, PHY-140/PHY-150, ORG-210 six-practical checkpoint
F. Molecules of life 41–48 ORG-220/ORG-230, BCH-210/BCH-220 structure-evidence gate
G. Integrated biochemistry 49–54 BCH-230, BCH-240 INT-304
H. Medicine-facing bridge 55–62 MED-310MED-330 INT-305, twelve-practical checkpoint
I. Route pathway 63–68 one PW-* (some pathways begin earlier) route gate, INT-306
J. Capstone 69–72 CAP-400, retention audit defence and completion review

Pathways with 180–240 hours normally start during blocks F–H or extend the route by 4–8 weeks. Recovery weeks are included approximately after weeks 12, 24, 36, 48, and 60 and should contain no new required concepts.

19.2 Part-time 96-week route (17–18 hours/week)#

Use the same dependencies, stretching each eight-week block to roughly eleven weeks and reserving every twelfth week for recovery/integration. Complete at least two short retrieval contacts per week; avoid a single long weekly session. Practicals may be batched into supervised weekends.

19.3 Accelerated route#

An accelerated 48–56 week route is suitable only after diagnostics demonstrate secure prior science and the learner can sustain 28–34 hours/week. Acceleration removes repeated instruction, never outcomes, practical evidence, spaced retention, or capstone defence.

19.4 Workload model#

The 1,440-hour common-core/bridge estimate is approximately:

Activity Hours Share
Source study and worked examples 360 25%
Retrieval and deliberate practice 230 16%
Quantitative/problem sets 260 18%
Practical/simulation/data investigations 230 16%
Cases, discussion, and integration 150 10%
Assessments, revision, and capstone 150 10%
Planning, feedback, and reflection 60 4%

These are planning estimates, not seat-time requirements. Fast completion of a mastered node does not require artificial time filling; struggling learners receive extra practice without penalty.

20. Teaching team and delivery requirements#

20.1 Learner equipment and accounts#

Required access is limited to a current standards-compliant browser; stable enough connectivity to download text/low-bandwidth packages; an email or privacy-preserving notification channel; a scientific calculator; paper or digital notebook; and spreadsheet software capable of formulas, plots, and CSV import/export. A local/offline package must preserve readings, transcripts, prompts, and progress sync where feasible. Programming is not required in the common core.

Physical practicals use a published, low-cost kit list and local household/school equipment only after risk review. No learner must purchase a microscope, sensor, chemical kit, commercial textbook, test-prep subscription, or AI subscription to earn the standard online completion. Costs and supervision requirements are disclosed before pathway selection.

20.2 Course operations#

  • There are no late penalties in the self-paced route. Cohort deadlines organize feedback access, but an equivalent later window remains available.
  • Learner questions receive an acknowledgement within two working days and substantive instructional feedback within five working days when human support is included.
  • Assessed artefacts receive rubric-linked feedback. A gate result must identify the exact weak nodes and a feasible next action.
  • Planned service outages, source withdrawals, and substantive corrections are shown in the learner record; progress data can be exported before migration.
  • Learners can report content, safety, accessibility, privacy, or conduct concerns without exposing the report publicly.
  • Harassment, discriminatory conduct, unsafe practical pressure, falsification, and retaliation are incompatible with participation. Sanctions require a reviewable process and preserve access to the open learning content where safety permits.

20.3 Teaching roles#

A credible implementation requires more than generated lessons:

  • curriculum lead: owns outcome map, versioning, assessment blueprint, and cross-domain coherence;
  • domain editors: Biology/Biochemistry, Chemistry/Organic, Physics/Quantitative, Behaviour/Society, and Human Physiology;
  • practical lead: approves risks, modalities, local-supervision standards, equipment lists, and safety-critical gates;
  • assessment editor: maintains parallel forms, rubrics, item statistics, bias review, and standard setting;
  • accessibility reviewer: audits content and assessments before release;
  • source/rights steward: maintains provenance, license ledger, source freshness, and correction trail;
  • learner support/tutors: perform misconception diagnosis, capstone supervision, authorship checks, and re-entry planning;
  • medical/ethics reviewer: checks medicine-facing contexts for scope, harm, stereotyping, and accidental advice.

AI may draft or review at scale, but high-risk safety, medical framing, assessment standards, and disputed claims require named human accountability before publication.

Recommended cohort support is one facilitated tutorial of 8–16 learners per week, plus monthly practical clinics. Fully self-paced learners receive equivalent asynchronous discussion and scheduled assessor access.

21. Learning resources and adoption rules#

21.1 Primary alignment resources#

21.2 Teaching-material candidates#

No resource is “the course.” Editors select at node level, verify currency and accessibility, declare what a resource does not cover, and supply an alternative modality. Resource availability is checked at least annually and before a high-stakes route cohort begins.

21.3 Resource-selection checklist#

Adopt or link an asset only when it has: exact scope match; named author/provider; stable URL or archived/versioned identifier where lawful; publication/update date; source citations; accessible alternative; no uncorrected material error; appropriate depth; acceptable privacy/tracking behavior; and license/terms compatible with the intended use. “Free to view” is not permission to adapt or redistribute.

22. Source alignment and design rationale#

Curriculum choice Evidence basis Design judgment / boundary
Biology, general chemistry, organic chemistry, algebra-based physics, first-semester biochemistry Reconciled 3/3 report spine; official MCAT depth; QAA access breadth Required common core; does not imply every system requires every course.
Quantitative reasoning, experimental design, data/statistical reasoning MCAT science-skills weighting; AP practices; A-level practical/quantitative work; QAA numerical-data outcomes Distributed spine and 20% practical portfolio, not a one-off methods unit.
Statistics before calculus Repeated reasoning evidence; MCAT mathematics excludes calculus Intro probability/inference required; calculus pathway optional.
Human physiology/homeostasis Strong medicine-facing value, MCAT organ-system content, QAA Human Biology breadth Required EK-BRIDGE; explicitly not labelled universal entrant minimum.
Immunity and biotechnology MCAT/Spanish Biology and medicine-facing relevance Required bridge at introductory depth; no clinical recommendations.
Psychology/sociology Full MCAT domain but weak as global requirement PW-US, not portable common core; supplied behavioural primer supports INT-306 for others.
Ecology Broad school Biology (AQA/AP); no ecology block in Spain's second-year Biology; absent from MCAT and weak as premedical minimum PW-BIO only; not attributed to MCAT and not attributed to spain-bach-pau.
Plant structure, transport, signalling and reproduction Broad school Biology (AQA/AP); RD 243/2022 has no broad plant unit; absent from MCAT PW-BIO only; not attributed to MCAT and not attributed to spain-bach-pau.
Photosynthesis Broad school Biology and RD 243/2022 autotrophic anabolism; absent from MCAT PW-BIO plus spain-bach-pau/ES-220; photosynthesis not falsely attributed to MCAT.
Evolution Broad Biology and present in MCAT; absent from Spain's second-year slice Required within Biology, with route-specific review.
Organic mechanisms/synthesis/spectroscopy Cross-system but depth uneven Common core bounded to biologically relevant mechanisms, short supplied sequences, and introductory evidence; advanced synthesis excluded.
Physical laboratory evidence A-level practical endorsements, AP inquiry emphasis, US/QAA laboratory expectations Twelve investigations; modality disclosed; online simulation never presented as hands-on equivalence.
Retakeable gates EmbeddedKnowledge anti-exam mission Retains unseen transfer and safety standards while removing one-shot judgment.
Route audits Admissions volatility and jurisdictional divergence Learner verifies named current institutions; course never promises eligibility.

23. Quality assurance and revision#

23.1 Release gates#

A module moves from draft to learner-facing only when:

  1. every outcome maps to at least one teaching asset, practice item, gate item, prerequisite, and stated exclusion;
  2. a domain editor verifies factual accuracy against primary or high-quality scholarly sources;
  3. a separate reviewer checks the gate against the outcome and difficulty blueprint;
  4. accessibility and bias checks pass;
  5. practical hazards and data/privacy implications are approved;
  6. all third-party assets have a rights-ledger entry;
  7. at least one novice and one prepared learner complete a usability pilot;
  8. corrections have public version history.

23.2 Monitoring#

Monitor node-level success, hint dependence, time-on-task ranges, high-confidence misconceptions, gate-form comparability, retention, accessibility failures, adverse/safety reports, and withdrawal points. Do not optimize for clicks, streak length, or rapid completion at the expense of retention or well-being.

Suggested triggers for review are: >20 percentage-point performance difference between equivalent gate forms; >30% of prepared learners failing the same non-intentional item; a subgroup gap unexplained by prerequisite evidence; any credible safety issue; a primary source/version change; or a substantiated content flag.

23.3 Correction severity#

  • C1 editorial: wording, accessibility, broken link; no scientific conclusion changes.
  • C2 substantive: explanation or assessment ambiguity; affected learners are notified and evidence re-evaluated if needed.
  • C3 safety/factual: could cause unsafe action or materially false learning; content is withdrawn, linked nodes frozen, learners notified, and expert/source adjudication required before restoration.

Annual review covers admissions links, source versions, route definitions, resource availability/licenses, and aggregate evidence. A generational AI re-audit may propose changes but cannot silently overwrite published content or learner records.

24. Boundaries and completion interpretation#

Completion means the learner has demonstrated this version's outcomes under the stated conditions. It does not establish:

  • eligibility for any particular medical school;
  • equivalence to named school qualifications, university credits, laboratory endorsements, QAA credit, or an MCAT/UCAT/PAU score;
  • clinical competence, permission to treat, or reliability of personal medical decisions;
  • mastery of ecology/plant science, calculus, advanced synthesis, programming, or another optional pathway unless recorded;
  • permanent retention without continued practice.

The honest next step after Premed is a learner-specific readiness review: inspect retained nodes, verify the current target institution or next-course requirements, and prescribe only the missing bridge—not repeat the entire syllabus.

Appendix A — Misconceptions that must be directly tested#

ID Misconception Disconfirming performance
MIS-01 heavier/faster objects experience a different gravitational acceleration under the same ideal conditions predict and explain controlled motion data
MIS-02 force is required to maintain constant velocity free-body/model comparison
MIS-03 pressure and flow are interchangeable reason through a changed resistance/radius scenario
MIS-04 equilibrium means equal concentrations or stopped reactions particle/model and Q versus K task
MIS-05 a catalyst changes equilibrium or reaction free energy energy diagram plus equilibrium evidence
MIS-06 spontaneity means fast contrast thermodynamic and kinetic data
MIS-07 pH is linear and buffers keep pH perfectly fixed logarithmic and buffer-capacity calculations
MIS-08 oxidation always adds oxygen; reduction always removes it electron/oxidation-state account
MIS-09 dominant means common, stronger, or better pedigree/population counterexample
MIS-10 one gene normally determines one trait or one protein regulatory/alternative processing and polygenic examples
MIS-11 evolution is purposeful improvement of individuals population-level selection explanation
MIS-12 enzymes create energy or make impossible reactions favourable free-energy/coupling and rate distinction
MIS-13 membranes are static walls and diffusion stops at equal amount dynamic/electrochemical equilibrium model
MIS-14 ATP is long-term stored energy or has uniquely “high-energy bonds” in isolation coupled-reaction and storage comparison
MIS-15 respiration means only breathing distinguish cellular and organismal processes and connect them
MIS-16 all microbes are pathogens; antibiotics treat viruses classification/mechanism scenario
MIS-17 immunity is simply stronger or weaker response-type, specificity, tolerance, timing model
MIS-18 a sensitive test makes a positive result probably true regardless of prevalence natural-frequency predictive-value task
MIS-19 statistical significance proves importance, causation, or truth effect/interval/design critique
MIS-20 no significant result proves no effect power/interval and equivalence-language task
MIS-21 correlation, a plausible mechanism, or an animal experiment alone establishes human causation evidence-chain comparison
MIS-22 uncertainty is a mistake that should be hidden measurement and conclusion audit
MIS-23 an anatomical or population average defines what is normal for every person variation and construct critique
MIS-24 a fluent AI answer or prestigious source is self-validating source triangulation and citation verification

Appendix B — Minimal learner portfolios#

By completion, the private learner workspace contains:

  • a mastery ledger and dependency view;
  • a dated error log with at least five documented misconception recoveries;
  • a quantitative portfolio covering units, graphs, probability, diagnostic tests, inference, and model critique;
  • twelve practical reports with raw evidence and modality labels;
  • six integration-studio artefacts;
  • six introductory primary-paper appraisals across at least four domains;
  • an institution/route audit with retrieval dates;
  • a capstone reproducibility package and correction memo;
  • a final 30-day study-maintenance plan.

Appendix C — Versioning convention#

Topic IDs remain stable when wording is clarified. A changed scientific outcome receives a new ID or version suffix and a migration note. This syllabus uses semantic versions:

  • patch (1.0.x) for links/editorial/accessibility changes without outcome changes;
  • minor (1.x.0) for added optional topics, resources, or assessment forms;
  • major (x.0.0) when required outcomes, pathways, or mastery standards change.

Learner records always retain the curriculum version under which evidence was earned.