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Submit a Drug for CDR Review

CADTH Collaborative Workspaces

The submission or submission requirements must adhere to the content, formal and organization in the current version of the Submission Guidelines for the CADTH Common Drug Review and applicable CDR Updates.

To submit and contribute drug review information you must be registered with the CADTH Collaborative Workspaces. If you are a drug manufacturer or designated consultant who intends to file a CDR application you may register by submitting completing the Registration Form.   

If you have already registered, you may log in.

Registration

Before submitting to the Common Drug Review, manufacturers or designated consultants must be registered with CDR. This will provide access to a secure submit and contribute page and enable the electronic delivery of documents to CADTH.