Consultation on the Draft Guidance Document: Licensing Requirements for Implantable Medical Devices Manufactured by 3D Printing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 hc.policy.bureau.enquiries.sc@canada.ca 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 The input gathered through this process will be used to finalize the Draft Guidance Document: Licensing Requirements for Implantable Medical Devices Manufactured by 3D Printing.

Contact us

Bureau of Policy, Science and International Programs
Therapeutic Products Directorate
Health Products and Food Branch
Health Canada
Holland Cross, Tower B
1600 Scott St.
Address Locator 3102C3
Ottawa, Ontario  K1A 0K9

Telephone: 613-948-4623
Email: hc.policy.bureau.enquiries.sc@canada.ca