Canadian Institutes of Health Research
570,556 snapshots · latest May 3, 2026
Homepage:https://cihr-irsc.gc.ca/
Archive explorer
Browse & search snapshots
Important note
Browse and search historical snapshots. This is an archive — not current guidance or medical advice. Archived content may be incomplete, outdated, or superseded. For up-to-date recommendations, always consult the official source website.
For background on coverage and capture methods, see Methods & coverage.
Browse archived sites
Health Canada
386,223 snapshots · latest Apr 14, 2026
Public Health Agency of Canada
243,880 snapshots · latest Apr 28, 2026
Clinical Trials Phase I-III clinical trials involving natural health products on human subjects must be authorized by Health Canada's Natural and Non-prescription Health Products Directorate (NNHPD) before commencement of the trial. This process requires the sponsor or a…
Policies The Natural Health Products Directorate (NHPD) has changed its name to the Natural and Non-prescription Health Products Directorate (NNHPD) subsequent to its recently expanded mandate to include the oversight of non-prescription and disinfectant drugs in addition to…
Natural health product licensing Information on applying for a natural health product licence, including access to ingredient and licence databases. Services and information Licensed Natural Health Product Database Search for product names, licence holders, licensed product…
Natural Health Products Online Solution Natural Health Products Ingredients Database The Natural Health Products Ingredients Database is a repository of scientific terminologies and Pre-cleared Information approved by the Natural and Non-prescription Health Products Directorate…
Contact Information Pharmaceutical Drugs: Clinical Trial Applications Office of Clinical Trials Therapeutic Products Directorate 5 th Floor, Holland Cross, Tower B A/L 3105A 1600 Scott Street Ottawa, Ontario Canada K1A 0K9 Tel: (613) 941-2132 FAX: (613) 952-9656 Clinical Trial…
Compliance and enforcement of medical devices - Forms, guidance, policies and laws Forms Recall reporting for medical devices: Medical device initial recall reporting form (FRM-0360A) Medical device final recall reporting form (FRM-0360B) Complaint reporting for medical devices:…
Clinical Trials For Natural Health Products The Natural Health Products Directorate (NHPD) has changed its name to the Natural and Non-prescription Health Products Directorate (NNHPD) subsequent to its recently expanded mandate to include the oversight of non-prescription and…
Post-Authorization Requirements Once an application has received regulatory authorization, the sponsor is required to inform Health Canada of the following: Clinical Trial Site Information If clinical trial site information was not available at the time of application, a…
Déclaration d'effet indésirable relié à un produit Si vous éprouvez présentement un effet indésirable, communiquez avec votre médecin, votre centre de santé communautaire ou l' Association canadienne des centres antipoison . Qui peut déclarer un effet indésirable? Les fabricants,…
Reimbursing a sperm or ova (egg) donor or a surrogate for expenditures related to donation or surrogacy In Canada, it is illegal to purchase sperm or eggs from a donor (or person acting on behalf of a donor) or pay a female person to be a surrogate. However, donors and surrogates…
Early release: coverage and features are still expanding.
