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Health Canada Investigational Testing Requirements under Part 3 of the Medical Devices Regulations: tips and beyond…

June 20 @ 5:30 pm - 8:30 pm

(America/Toronto)    $25.00 – $40.00

Medical devices are a big part of clinical research in Canada.  Join us on June 13 when Amanda Jones from the Medical Devices Directorate discusses upcoming changes to the regulations and other key information you need to know!

Agenda in EST:

5:30 pm –In person attendees arrive

6:00 pm – Dinner and Networking

6:45 pm – Virtual Attendees log in – link to be sent

7:00 pm – Presentation begins 

8:30 pm – Event concludes

Learning objectives:

  1. Learn when to submit a clinical trial application for medical devices (Investigational Testing requirements under Part 3 of the Medical Devices Regulations)
  2. Discover the obligations for manufacturer/importers and the study investigators
  3. Utilize tips for submissions to avoid to help speed up the efficiency of your applications
  4. Have your common questions answered

Details

Date:
June 20
Time:
5:30 pm - 8:30 pm (America/Toronto)
Cost:
$25.00 – $40.00
City:
,

Venue

Virtual online via Zoom Webinar

Speaker

Amanda Jones, MSc.: 20Jun2024 Health Canada Medical Devices

» view speaker's bio

Tickets

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