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Fees in Respect of Drugs and Medical Devices Regulations

Jun 17, 2019 ...) The purpose of these Regulations is also to remit, in whole or in part, certain of those fees. Application Marginal note:Non-application 3 These Regulations do not apply in respect of (a) a drug that is for veterinary use only; (b) a drug that is a natural health product; (c) a drug that is the subject of an extraordinary use new drug submission filed under section C

Section I: Table of regulations, statutory instruments (other than regulations) and other documents—June 30 2019

Aug 26, 2019 ... Act, 2001 Ancillary Activities (Insurance Companies, Canadian Societies and Insurance Holding Companies) Regulations Insurance Companies Act Anhydrous Ammonia Bulk Storage Regulations (General Order No. O-33) Canada Transportation Act Animals of the Family Bovidae and Their Products Importation Prohibition Regulations Health of Animals Act Annex Code 9075

Memorandum D19-9-2 -Importation and Exportation of Cannabis, Controlled Substances and Precursors

Dec 24, 2018 ... or exportation of narcotics or controlled drugs for animals. This exemption does not apply to products containing substances listed in Annex I to this exemption, unless they have been approved by Health Canada for market in Canada under the FDR or approved for market in the country from which the product is being imported by the corresponding regulatory authority

Jobs, Growth and Long-term Prosperity Act

Nov 15, 2019 ... of Part 4 amends the Food and Drugs Act to give the Minister of Health the power to establish a list that sets out prescription drugs or classes of prescription drugs and to provide that the list may be incorporated by reference. It also gives the Minister the power to issue marketing authorizations that exempt a food, or an advertisement with respect to a food

Consulting with Canadians

Sep 5, 2019 ... Advertising/Marketing Agriculture Amendments Animals Children Communication Copyright/Trademarks/Patents Culture Development Economy Economic development Employment Environment Education Exporting/Importing Financial assistance and entitlements Food and drug Finance Foreign affairs Fisheries Government procurement Housing Heritage Human resources Health Immigration

Consulting with Canadians

Sep 5, 2019 ... feedback, visit the CNSC website. Consultation on Pyriproxyfen and Its Associated End-use Products, Proposed Re evaluation Decision PRVD2019-10 Open - accepting input Health | Policy Nov 6, 2019 to Feb 4, 2020 2019-11-06 2020-02-04 Health Canada Health Canada is consulting Canadians on the proposal to continue registration for all uses of pyriproxyfen, with label

Travel advice and advisories for France

Dec 6, 2019 ... at least one parent must be in possession of an authorization to leave the country signed by one of the parents, as well as a photocopy of the signing parent’s identification. More information and a copy of the authorization to leave the country form - French administration service (in French only) More about travelling with children Yellow fever Learn about

Draft Guidance Document: Applications for Medical Device Investigational Testing Authorizations

Oct 9, 2018 ... Directorate or Bureau within Health Canada, depending on the principal mechanism of action and hence the classification of the product. Refer to the guidance document entitled Drug/Medical Device Combination Products Policy (refer to Appendix 2). Authorization for the sale and importation of all investigational products to be used within a medical device clinical

Agricultural Growth Act

Nov 15, 2019 ... for exceptions to the application of those rights. It amends the Feeds Act, the Fertilizers Act, the Seeds Act, the Health of Animals Act and the Plant Protection Act to, among other things, (a) authorize inspectors to order that certain unlawful imports be removed from Canada or destroyed; (b) authorize the Minister of Agriculture and Agri-Food to take into account

Proposed Approach to the Regulation of Cannabis

Nov 21, 2017 ..., natural health products, medical devices, and cosmetics. The Act and its regulations regulate the safety, efficacy and quality of health products, such as prescription or non-prescription drugs, natural health products, and medical devices. Health products are subject to a review process before they are authorized for sale with health claims. While there is no pre

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