The drug and health products inspections database (DHPID)
On this page
- Why we created the DHPID and what it does
- Related forms, services and information
- Inspections guides and help links
Why we created the DHPID and what it does
The Drug and Health Products Inspections Database (DHPID) supports open government and regulatory transparency.
It:
- gives you access to information about each type of drug and health product inspection done by Health Canada, in Canada and abroad
- covers all inspections done since 2012, in Canada and abroad
- tells you what health product establishments are licensed or registered by Health Canada
- replaces the drug establishment licence live listing
This information is now:
- mobile and user-friendly
- designed to include up-to-date information
- organized on a single search platform for each inspection program
Related forms, services and information
- Drug and health products register
- Good manufacturing practices
- Good clinical practices
- Medical devices
- Cells, tissues and organs
- Blood
- Donor sperm and ova
Inspections guides and help
These documents give information that will help you understand regulated inspections processes.
- Terminology
- About drug inspections
- About clinical trial inspections
- About medical device inspections
- About good pharmacovigilance practices (GVP) inspections
- About cells, tissues and organs (CTO) inspections
- About blood inspections
- About donor sperm and ova inspections
Related links
Disclaimer
This web page does not constitute part of the Food and Drugs Act (the Act) or its Regulations. In the event of any inconsistency or conflict between the Act or regulations and these web pages, the Act or the regulations take precedence. These web pages are intended to provide access to information on inspections performed by different inspection programs in Health Canada.
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