Quality Assurance for Cannabis Certificate Program
December 4-7, 2019 | 9:00 AM- 5:00 PM
The quality department within companies is responsible for activities that have impact on the quality, safety or efficacy of the cannabis. It is also responsible for ensuring that all contracted services, which is more common today than ever before, are also verified to meet the quality standards set both by the company and the regulatory requirements.
| | December 6, 2019 | 9:00 AM-5:00 PM
- Definition and History of GMPs
- GMP & Drug Establishment Licencing
- The importance and requirements for adequate premises and equipment
- Personnel hygiene, training and responsibilities
- Quality Assurance versus Quality Control
| | Preparing for Health Canada Audits in the Cannabis Industry – A guide on how to successfully host regulatory audits
| December 13, 2019 | 9:00 AM-5:00 PM
- Regulatory Requirements for Audits under the Cannabis Act
- Objective of Health Canada Audits
- Types of Health Canada Audit
- Pre-Licence
- Routine Audits
- Unexpected Audits or “targeted” inspection
| | | January 8, 2020 | 1:00-3:00 PM
This webinar examines the history, rationale, purpose, and GMP requirements applicable to the manufacturing, packaging and labeling, testing, and control of pharmaceutical products and consequence of inaction. Gain practical knowledge in
| | | Cannabis Micro Licence Application Process and Requirements | December 11, 2019 | 2:00-3:30 PM
The Cannabis Act establishes that an application for one of the Micro Cultivation/Processing Licence must be filed with Health Canada in the form and
| | | | | Health Canada, GPP, and GMP Compliant Facility Design and Build | December 10, 2019 | 2:00-3:00 PM
Based on the recent announcement by Health Canada, prospective applicants of a cannabis cultivation, processing or medical sales licences are required to have fully built regulatory-compliant
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