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PLANTOGRAM · DOCTORS’ EDUCATION

Medicinal Cannabis Prescriber Training: Learning Structure

Explore a proposed foundation and advanced learning structure covering pharmacology, patient selection, access pathways, safety and clinical governance.

A structured learning pathway for doctors

This proposed training structure moves from foundational knowledge to more detailed clinical reasoning and governance. It is intended to organise learning, not to award legal prescribing authority or certify competence by itself.

The learning pathway has a foundation stream and an optional advanced stream.

Foundation stream: six learning modules

The foundation stream provides a way to identify the knowledge a doctor needs before considering an individual patient’s treatment.

ModuleLearning topics
1. Medicinal cannabis in AustraliaHistory, current landscape, evidence by indication, the endocannabinoid system, THC, CBD and product types.
2. Regulatory foundationsTGA access pathways, SAS-B, AP, established history of use, state or territory obligations, consent and records.
3. Patient selection and scopePrevious treatment, red flags, contraindications, clinical scope and individual risk–benefit assessment.
4. Categories and treatment matchingCannabinoid categories, dosage forms, composition and matching a format to a defined objective.
5. Safe prescribing fundamentalsAdverse effects, interactions, psychiatric risk, driving and individualised initiation and monitoring.
6. The first consultationAssessment structure, records, goals, clinical rationale, education and follow-up.

Advanced stream: seven learning modules

The advanced stream deepens knowledge for practitioners whose clinical scope and experience justify further learning. Progression should depend on demonstrated learning needs and competence, rather than time alone.

ModuleLearning topics
1. THC and CBD pharmacologyReceptor biology, pharmacology, routes and formulation differences.
2. Adverse effects and safetyCommon and serious harms, patient-specific risks and management.
3. Drug interactionsMetabolic interactions, sedating combinations and polypharmacy.
4. Psychiatric risk and selectionAssessment, high-risk presentations, consent and documentation.
5. Driving and impairmentClinical impairment, legal differences and patient counselling.
6. Dosing and titrationProduct-specific initiation, changes in exposure and special populations.
7. Monitoring and governanceBaseline outcomes, review, records, reporting, treatment modification and cessation.

Course completion and AP status are separate

Education can support clinical preparation, but TGA authorisation is a separate process. Eligibility for the established-history-of-use pathway depends on the applicable product, dosage form, indication and patient criteria.

How the learning structure can be used

Start by identifying learning gaps, then work through the relevant modules and official references. Use clinical cases to practise recording an indication, comparing alternatives, identifying risk and setting measurable review criteria.

The structure is designed primarily for doctors. Other practitioner groups must follow their own scope, eligibility and professional requirements; a shared educational resource does not make their access pathways identical.

References and further reading

Related resources