Discover the latest regulations for Medical Device approval and enhance your knowledge!

Register for the Webinar!

Happening Next Week! Greetings! Harmonization of the regulatory requirements between Health Canada, the FDA and other regulatory bodies, including the new Medical Device Single Audit Program (MDSAP), is continuously evolving and is intended to reduce the regulatory burden on both the manufacturers and the regulators. REGISTER NOW!   The following topics will be covered during the Workshop: ITA submission Licensing application Establishment of Quality Management Systems Risk management LEARN MORE! Date and Time: June 7, 2023 9:00 AM - 5:00 PM (EST) How is the webinar delivered? Online. Live, Interactive, Instructor-led Get Certified Today Interested in this workshop? Register today by calling our team at 416-502-2277 or email us at info@aaps.ca.

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