Open Government Portal
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 …
Present the list of new drug submissions (NDSs) that are currently being reviewed.
Understand the decisions to approve or not approve the sale of drugs and medical devices in Canada.
Drug shortages can occur for any number of reasons and can result from problems at any point in the drug …