Medical Device Quality and Regulatory Requirements for Importer/Distributor and Manufacturers – Canadian Market

Medical Device Quality and Regulatory Requirements for Importer/Distributor and Manufacturers – Canadian Market Abstract This intensive one-day comprehensive course, provides participants with a solid understanding of the principles behind the Medical Device Regulations and how to apply them to your company’s current processes and procedures. The course starts with a detailed overview of Medical Device Regulations and the requirements of Establishment which wishes to import / Distribute / Manufacture these medical products. Different business scenarios will b e highlighted such as Manufacturing, Importation, Distribution, Private labeling and even servicing will be touched upon. The course shares experiences from real life scenarios of companies wishing to handled Medical devices in the Canadian market and “Lessons learned” as well as “show-stopper” situations. Course Outline INTRODUCTION – Medical Device Regulations Explained Nne-Medical Device Regulations Mandatory considerations for the Canadian Market ISO 13485 – Brief description of when you would need this and what does it entail Business Scenarios – Considerations to be made if you are or with so be  Please click the link below to register. Date: November 29, 2019     Time: 9:00 a.m. - 5:00 p.m.     Registration Fee: CAD $685.00 + HST Program Details Location: AAPS Training Center 200 Consumers Road,  Suite 200 North York,  Ontario M2J 4R4 Canada Telephone: 416-502-2277 See what's happening on our social sites: ‌ ‌ ‌ ‌ Copyright ® 2019 Academy of Applied Pharmaceutical Sciences (AAPS) Inc.

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