Monday, March 6, 2023

Want to get your Medical Device approved? Learn the latest regulations here!

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.
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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:

April 5, 2023

9:00 AM - 5:00 PM (EST)


How is the webinar delivered?

Online. Live, Interactive, Instructor-led
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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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AAPS | 885 Sheppard Avenue West, Toronto, M3H 2T4 Canada
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