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Pages in category "Medical and health organizations based in Canada" The following 20 pages are in this category, out of 20 total. This list may not reflect recent changes .
Health Canada (HC; French: Santé Canada, SC) [NB 1] is the department of the Government of Canada responsible for national health policy.The department itself is also responsible for numerous federal health-related agencies, including the Canadian Food Inspection Agency (CFIA) and the Public Health Agency of Canada (PHAC), among others.
Hears appeals regarding decisions made by regional health authorities, such as the issuance, cancellation, suspension, or refusal to issue licenses or permits. Health: Tribunal Roster of Public Members under the Health Professions Act Regulatory/Adjudicative List of public members who may be selected to sit on complaint review committees and ...
Health regions, also called health authorities, are a governance model used by Canada's provincial and territorial governments to administer and deliver public health care to all Canadian residents. Health care is designated a provincial responsibility under the separation of powers in Canada's federal system. Most health regions or health ...
Pages in category "Government health agencies in Canada" The following 6 pages are in this category, out of 6 total. This list may not reflect recent changes. A.
A stringent regulatory authority is a regulatory authority which is: a) a member of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), being the European Commission, the US Food and Drug Administration and the Ministry of Health, Labour and Welfare of Japan also represented by the Pharmaceuticals and Medical Devices Agency (as before ...
Financial regulatory authorities of Canada (1 C, 16 P) H. Health Canada (37 P) P. Public utilities commissions of Canada (7 P) S. Self-regulatory organizations in ...
On 25 March 2011 [5] and after the pH1N1 pandemic, [3] amendments were made to the Food and Drug Regulations (FDR) to include a specific regulatory pathway for EUNDs. Typically, clinical trials in human subjects are conducted and the results are provided as part of the clinical information package of a New Drug Submission (NDS) to Health Canada ...