This free workshop offers an introduction to the role of a Quality Assurance Person (QAP) in a cannabis facility. Participants will gain an understanding of the core responsibilities, regulatory requirements, and best practices for ensuring compliance with cannabis industry standards. The session will cover the importance of quality control in cannabis production, including testing, documentation, and adherence to Good Manufacturing Practices (GMP). Attendees will also learn about the key areas of focus for QAPs in cannabis, including batch release, product traceability, sanitation plans, creating a recall and complaint system and maintaining high standards throughout the cultivation and processing operations.
This workshop is ideal for professionals interested in working in the cannabis industry, particularly those in or aspiring to Quality Assurance roles. It is beneficial for individuals in regulatory affairs, quality control, compliance, and those seeking to understand the role of QAPs in maintaining product quality and safety in cannabis production.
This workshop covers the following topics:
Gain a foundational understanding of the QAP’s role within a cannabis facility and the essential responsibilities associated with maintaining quality standards.
Become familiar with Cannabis Industry Regulations & Interpret Regulatory RequirementsDescribe the key provisions of the Cannabis Act and Cannabis Regulations, with particular emphasis on Part 5 – Good Production Practices (GPP).
Demonstrate GPP ComplianceDevelop and implement facility, equipment, sanitation, and personnel hygiene controls that meet the specifications of Sections 80–84 of Part 5.
Investigate Deviations, Complaints & RecallsAnalyze non-conformances, lead corrective and preventive action (CAPA) initiatives, and execute product complaint investigations and recall procedures.
Foster a Quality CultureTrain, coach, and evaluate production staff on GPP, SOP adherence, and hygiene practices, reinforcing the principle that “if it’s not documented, it didn’t happen.”
Certificate of attendance available upon request.
Note: Registration closes one week prior to the start of workshop. Workshop registration is intended for individual use only. Each registration grants access to one participant. If you plan to attend as a group or company team, please ensure that each participant is registered separately. Group rates and corporate packages are available—contact us for details.
Refunds are only available if cancellation is requested at least 48 hours before the workshop. No refunds will be issued for late cancellations.
Pharma, Cannabis
Bilal Al-Kadri is a highly skilled Quality Assurance and Compliance expert with over two decades of proven leadership in the pharmaceutical, medical, veterinary, and cannabis sectors across North America and the Gulf region. As General Manager and Quality Assurance Person at EU Relief in Toronto, he spearheads all facets of cannabis operations, ensuring excellence in cultivation, processing, and regulatory adherence.
Recognized for his deep regulatory expertise, Bilal is proficient in Canadian GMP, cGMP (21 CFR Parts 210 & 211), Good Production Practices, ICH guidelines, ISO standards, and OSHA requirements. His extensive experience includes senior roles at top-tier organizations such as Sundial Inc. (Former Zenabis), CannaPiece, Summit Veterinary Pharmacy, and Apotex, where he led regulatory audits, product releases, CAPA systems, training initiatives, and the development of robust global quality systems.
Complementing his industry work, Bilal is also a dedicated educator, teaching advanced courses at AAPS. He holds a B.Sc. in Applied Chemistry and Biology, along with a post-diploma in Pharmaceutical Quality Assurance and Quality Control.
