UPCOMING LIVE WEBINAR -Health Canada, GPP, and GMP Compliant Facility Design and Build

Live Webinars Health Canada, GPP, and GMP Compliant Facility Design and Build December 10, 2019 | 2:00 PM-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. It is now imperative that your site and floor design is regulatory compliant prior to build-out. Additionally, in order to obtain GMP compliant status from the European regulatory agencies, specific building design and materials for your operational area are required. More Details  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 More Details GMP Fundamentals 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 More Details Sanitation Program for Cannabis Production – Cannabis Act January 9, 2020 | 2:00-3:30 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. More Details Workshops 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 More Details 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 More Details Consulting and Training Services Most importantly, AAPS custom tailors the consulting solutions to fit your needs. We work side-by-side with you to create solutions that help you achieve what you want to achieve. See what's happening on our social sites: ‌ ‌ ‌ ‌

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