Last Chance to Register! Live Interactive Workshop - 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 What is the webinar about? Medical Device Regulations and how to apply them to your company’s current processes and procedures. How is the webinar delivered?: Live, interactive, instructor led  Date and Time: May 8, 2020 | 9:00 AM - 5:00 PM Cost and Location: $685+HST | Online Who should attend: This One-day course is applicable to Personnel from the following areas: Regulatory Affairs, Quality Assurance, Validation, Quality Control Laboratory, Analytical Laboratory, Training, Contract Laboratory, Consultants, Manufacturing, Packaging and Labeling, Distributers and Wholesalers, Importers. How do I register? REGISTER HERE  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 be highlighted such as Manufacturing, Importation, Distribution, Private labeling and even servicing will be touched upon. Course Outline: ◆ Introduction ◆ Medical Devices risk-based classification ◆ Requirements for Manufacturers/Importers/Distributers ◆ Special types of medical devices ◆ Medical Device licence application ◆ Quality Management Systems (QMS) requirements ◆ Additional Canadian market requirements  For more information please visit: www.aaps.ca or contact @416-502-2277 See what's happening on our social sites: ‌ ‌ ‌ ‌

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