Certificate Pathway
Follow a structured learning experience focused on the knowledge and practices described for this program.
Study the Quality Assurance Person’s oversight responsibilities across production, records, investigations, release decisions, and compliance systems.
Program delivery and scheduling depend on the selected intake. Refer to the current Program details above and confirm availability with Admissions.
Study the Quality Assurance Person’s oversight responsibilities across production, records, investigations, release decisions, and compliance systems.
The training connects cannabis operations with quality systems, controlled documentation, risk-based decisions, and regulatory awareness.
What this program can offer
Follow a structured learning experience focused on the knowledge and practices described for this program.
Build understanding through focused lessons covering the core themes, terminology, workflows, and documentation of the subject.
Connect the training with the expectations, responsibilities, and quality practices encountered in relevant workplaces.
Work through guided examples, scenarios, records, and problem-solving activities appropriate to the program topic.
Available delivery formats and schedules depend on the selected intake and are shown in the current Program details.
Understand the focus and learning context
The Quality Assurance for Cannabis Certificate Training Program provides comprehensive technical knowledge and practical skills required to ensure cannabis products are safe, compliant, and suitable for sale or distribution under the Cannabis Act and Regulations.
Recognized by leading industry and regulatory bodies across Canada and internationally, this program equips participants to develop and implement Good Production Practices (GPP), Quality Assurance (QA) programs, and Quality Management Systems (QMS).
Trainees will learn essential aspects such as record keeping, complaint handling, recall procedures, sanitation, audits, inspections, and quality control, alongside procedures for product approval or rejection, sampling plans, test methods, and change control including CAPA and gap analysis.
Core topics for this program
Review independence, authority, responsibilities, escalation, and cross-functional communication.
Examine records, specifications, test results, deviations, complaints, and disposition considerations.
Connect procedures, training, document control, CAPA, change control, and risk management.
Organize evidence, conduct internal checks, respond to observations, and monitor corrective actions.
Build a practical foundation
Explore the current learning topics
Quality Assurance Systems for Cannabis Module 2 Overview of GxP for Cannabis: Good Production Practices (GPP) Cannabis Eu-GMP Good Agriculture and Collection Practices (GACP) Good Manufacturing Practices (GMP) Preventive Control Plans (PCP) Hazard analysis and critical control points (HACCP) Good Validation Practices (GVP) Good Clinical Practices (GCP) Good Laboratory Practices (GLP) Good Documentation Practices (GDP) Safe Food for Canadians Regulations (SFCR) Module 3 Quality Management Systems QMS Programs and Policies: Control Procedures Sanitation Program Pest Management Program Calibration Program Validation Program Training Program Audit and Inspection Programs Other QMS programs Module 4 Good Production Practices (GPP) for Cannabis (GDocP) GPP regulatory requirements and applications for: Sales/exports SOP Building Equipment Filtration system Sanitation Program Cannabis Testing Quality Assurance Person (QAP) Module 5 EU-GMP — GPP Gap Analysis Case studies Day 3 – Sanitation and Testing Requirements for Cannabis Production Module 1 Cannabis regulatory sanitation requirements Expectation and current guidance Objectives of Cleaning and Sanitation Approved list of detergents and sanitizers Module 2 Cleaning and Sanitation Program for production Cleaning and Sanitation Procedure (SOP) for storage Cleaning and Sanitation Procedure (SOP) for extraction Module 3 Self-Inspection Procedure Cleaning and Sanitation Records Cleaning and Sanitation Verification Module 4 Deviation, Out of Specification and CAPA Training of personnel and record keeping Cleaning validation requirements Cleaning validation approaches for better performance Module 5 Pest Control Management Case study Analytical Testing Requirements Biological Testing Requirements Physical Testing Requirements Stability Studies Mandatory and Non-Mandatory Testing Module 6 Testing Specification Appropriate Testing Instrument and Software Systems Method Development and Validation Module 7 Out of Specification (OOS) Training Requirements Packaging, Labeling and Shipping Case Study Day 4 – Technical Writing and Audit/Inspection Programs for Cannabis Module 1 Cannabis Current Audit and Inspection Audits (internal and external) Self-inspection programs for process improvements CRA audit and walk-through Regulatory Inspections Preparing for inspections Corrective and preventive actions Case Study — Create Template Module 2 Cannabis Technical Writing — Part 11 Good Documentation Practices (GDP) Training Requirements Quality Deviation Reports (QDR) Standard Operating Procedures Module 3 CAPA and Gap Analysis — Part 2 Process maps and data trending Risk management Module 4 Change Control and Related Topics — QA Part 3 Change Control Process Case Study
Select a course to view its description.
Support from inquiry through completion
Study practical concepts and workplace context connected to the program subject.
Learn with instructor support and opportunities to ask questions about the course material.
Ask Admissions about current online, live, recorded, hybrid, or on-campus availability.
Receive guidance about eligibility, schedules, fees, registration, and the documents needed for your intake.
Consider whether the training matches your goals
Confirm your eligibility and documents
Connect training with relevant work environments
Speak with Admissions about the current intake, delivery format, tuition, prerequisites, and registration steps for Quality Assurance Person(QAP).
What to know before you apply
Study the Quality Assurance Person’s oversight responsibilities across production, records, investigations, release decisions, and compliance systems.
The current duration is displayed in the Program details above. Confirm the schedule and completion timeline for your selected intake with Admissions.
Available online, live, recorded, hybrid, or on-campus formats vary by program and intake. Use the current delivery information above and confirm the scheduled format before registering.
Requirements vary by credential and applicant background. Contact Admissions for the current eligibility criteria and document checklist.
Contact Admissions for the current course sequence, topic details, schedule, and any program-specific practical requirements.
No. Employment, certification, licensing, scope of practice, and role eligibility are determined by employers and applicable authorities. Confirm requirements for your intended pathway.