UPCOMING LIVE WEBINAR -Live Webinar Cannabis Micro Licence Application Process and Requirements

Live Webinars Cannabis Micro Licence Application Process and Requirements December 11, 2019 | 2:00 PM-3:30 PM  Although security requirements are less demanding in comparison to obtaining a Standard Cultivation/Processing Licence, the application process to acquire a Micro Licence under the Cannabis Act can still be complicated and requires undergoing a strict and thorough review by Health Canada. Applicants must ensure that the information provided in the application is detailed and accurate and clearly demonstrates that they are compliant with all the requirements of the Act. More Details  Sanitation Program for Cannabis Production – Cannabis Act January 9, 2020| 2:00-3:30 PM It is therefore extremely important to understand the fundamental principle of sanitation procedures and to implement and use these procedures effectively. Lack of proper and validated cleaning 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 GMP and GACP for the Cannabis Industry January 15, 2020 | 2:00-4:00 PM Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any production that cannot be eliminated through testing the final product. 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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