Medical Device Quality and Regulatory Requirements for Importer/Distributor and Manufacturers – Canadian Market Workshop
Workshops
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.
This workshop will explain the importance of adverse drug reactions, the Canadian MEdEffect Scheme, the source of adverse drug reaction reports and the differences between serious and non-serious events.
Ina addition, a MedEffet form will be completed in class.
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.
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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