Consultation on the Draft Guidance Document: Licensing Requirements for Implantable Medical Devices Manufactured by 3D Printing
From Health Canada
Current status: Closed
Opened on November 8 and will close to new input on January 8, 2019.
The purpose of the consultation is to seek stakeholder feedback on the technical considerations related to the licensing of 3D-printed devices.
Join in: how to participate
Send an email to Bureau of Policy, Science and International Programs at firstname.lastname@example.org with your ideas or comments to make yourself heard.
Who is the focus of this consultation
We will engage with the Medical Device Industry.
Feedback from the Consultation
Your ideas and inputs are sought around the licensing requirements for 3D-printed medical devices. The input gathered through this process will be used to finalize the Draft Guidance Document: Licensing Requirements for Implantable Medical Devices Manufactured by 3D Printing.
Bureau of Policy, Science and International Programs
Therapeutic Products Directorate
Health Products and Food Branch
Holland Cross, Tower B
1600 Scott St.
Address Locator 3102C3
Ottawa, Ontario K1A 0K9
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