Opened on November 24, 2021 and will close to new input on February 22, 2022.
Health Canada is pleased to announce the development of the Device Advice: Medical device meetings draft guidance document and associated documents. This guidance document is the result of a commitment to develop and implement processes that facilitate effective communication between medical device manufacturers and Health Canada.
We will engage with medical device stakeholders, primarily:
Health Canada would like you to participate by providing feedback with respect to the Device Advice: Medical Device Meetings Draft Guidance Document.
Your feedback is sought regarding the overall clarity and content of the draft guidance document, the meeting request form and the records of decision templates. Specifically, we would like to receive comments from medical device stakeholders on the following aspects of the documents:
We are also requesting that you test the meeting request form by sending mock content to help determine if adjustments are necessary to the form.
The input gathered through this process will be used to finalize the guidance document and the related content. The feedback will:
Medical Devices Directorate
Health Products and Food Branch
11 Holland Ave, Tower A
Address Locator: 3002A
Ottawa, ON K1A 0K9