Sanitation Program for Cannabis Production – Cannabis Act
January 9, 2020 | 2:00 PM-3:30 PM Good Production Practices (GPP) of the Cannabis Act mandates that Licensed Producers ensure the cleanliness of the premises and equipment. Having effective sanitation and pre-operational Inspection procedures can minimize the risk of contamination of your product, ingredients, processing aids, packaging materials, and product contact surfaces.
| | | | 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 manner specified by the Minister and must include the information required by
| | | 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 understanding of the essential
| | | | | | 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 facilities prior to the review and processing of the application.
| | | How to Write Effective Standard Operating Procedures (SOPs)
| January 15, 2020 | 9:00 AM-5:00 PM
Regulatory Agencies require written procedures for all systems and operations which impact the quality and safety of pharmaceutical products. SOPs provide the main forum for the documentation of a Company’s systems, processes and operations. SOPs are therefore the most popular documents audited by Regulatory Agencies during GMP inspections to ensure they reflect current practices that follow regulatory requirements and they
| | Batch Record Review and Investigation
| January 24, 2020| 9:00 AM-5:00 PM
- Regulatory Requirements for GMP Documents
- Basic Requirements and Techniques for Batch Record Review
- Techniques for Performing a Technical Review and Conducting Follow-Up Investigations
- Workshop – Review of a Mock Batch Production Record
- Documentation GMP and Regulatory Trends
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