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The Medical Devices Bureau of the Therapeutic Products Directorate (TPD) is the national authority that monitors and evaluates the safety, …
The term Medical Devices covers a wide range of health or medical instruments used in the treatment, mitigation, diagnosis or …
These inspection and investigation functions have as main objective to reduce risks to subjects enrolled in clinical trials, while encouraging …
We are updating how we disclose the clinical information used to assess the safety and effectiveness of drugs and medical …
Drug and medical device manufacturers submit clinical information to Health Canada for the approval of new products. Health Canada assesses …
Before a drug is authorized for sale in Canada, it must be issued a DIN in accordance with the Food …
These guidelines are meant to help companies in the drug manufacturing industry and health care professionals understand how to comply …
Health Canada's drug products fact sheet describes how drugs are reviewed in Canada including how drugs are developed and submitted …
How to access a list of generic drug submissions currently under review.
For eligible submissions accepted into review on or after October 1, 2018, the submission 'class' added to the Lists of …