Register Now! LIVE WEBINAR - Drug Product Submission (NDS) Preparation in CTD and eCTD format

Live Webinars Drug Product Submission (NDS) Preparation in CTD and eCTD format March 27, 2020 | 11:00 AM-3:30 PM The eCTD format has become mandatory in key markets for electronic submissions. Since January 2010, the European Medicines Agency has required all applications in the centralized procedure use the eCTD format. In the U.S., the More Details  Cannabis Retail Application Process and Requirements April 2, 2020 | 1:00-3:00 PM The Cannabis Act establishes that provincial, territorial and municipal governments will determine the More Details Conducting Effective Annual Product Review April 3, 2020 | 1:00-7:00 PM Annual Product Review (APR) is a critical cGMP requirement. It is an integral part of QA function, which provides an opportunity to assess the state-of-control More Details GMP Fundamentals April 8, 2020 | 1:00-3:00 PM This webinar examines the history, rationale, purpose, and GMP requirements applicable to the manufacturing, packaging and labeling, More Details Cannabis Micro Licence Application Process and Requirements April 9, 2020 | 2:00 PM-3:30 PM The Cannabis Act establishes that an application for one of the Micro 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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