Changes to notification requirements for biologic drugs: Notice to industry

Health Canada is reducing the administrative burden to help clinical trial sponsors and market authorization holders efficiently distribute treatments.

On this page

Purpose and background

The COVID-19 pandemic has created an unprecedented demand on Canada’s health system. Health Canada is implementing innovative and flexible measures to help prioritize and expedite the regulatory review of COVID-19 health products without compromising Canada’s high standard of safety. These measures will ensure that needed health products and medical supplies are available to Canadians and healthcare workers.

Measures to expedite the lot release of biologic drugs in groups 1A and 4

Effective immediately, clinical trial sponsors and market authorization holders are no longer required to provide fax-back notifications to the Biologic and Radiopharmaceutical Drugs Directorate prior to the distribution of certain biologic drug lots:

This change applies to biologic drugs:

Fax-back notifications are still required for:

For prophylactic vaccine lots to be used in clinical trials, a formal request for release, with the relevant lot release documentation, is still required.

We will share updates with sponsors as applicable. If you have any questions, please contact: hc.brdd.ora.sc@canada.ca

Report a problem or mistake on this page
Please select all that apply:

Thank you for your help!

You will not receive a reply. For enquiries, contact us.

Date modified: