The power to make Marketing Authorizations (MA) is an authority provided to the Minister of Health pursuant to sections 30.2 to 30.4 of the
Food and Drugs Act. MAs are ministerial regulations which enable the Minister to implement certain food safety decisions by exempting from prohibitions found in either the Food and Drugs Act or the Food and Drug Regulations. Additionally, MAs can be used to define classes, set conditions and incorporate documents by reference.
As regulations, MAs have the force of law and are enforceable as are any documents that are incorporated by reference into the MAs.
Related Information
The MA authority is a regulatory tool that the Minister of Health may choose to use to implement certain food decisions. Food industry stakeholders may put forward a submission to change some aspect of food regulation, which in turn may result in the amendment of an existing MA or the creation of a new MA.
MAs cannot be used to establish new prohibitions at the level of the Act or Regulations. They can only exempt. Furthermore, MAs are rules of general application, meaning that they apply to the entire food industry, as opposed to a single individual or company.
Even though they refer to sections of the Food and Drug Regulations, MAs are not part of or housed under the Food and Drug Regulations. They are their own separate regulations and are housed on the website of the Canada Gazette. Links to the current food MAs are available in the Table of Food Marketing Authorizations
As regulations, MAs are subject to the requirements of the Statutory Instruments Act (SIA) and the Cabinet Directive on Regulatory Management (CDRM). When creating a new MA or amending an existing MA, Health Canada must follow a formal regulatory process which includes review of the proposed MA by Justice Canada, public consultations on the proposed MA and final publication of the MA in the
Canada Gazette, Part II.
Since MAs are ministerial regulations, the entire regulatory development process, including review of the proposal against the CDRM, is managed by Health Canada (as opposed to the Treasury Board Secretariat), providing greater control over prioritization, approval timelines, consultation management and regulatory drafting. Additionally, final decisions are subject to Ministerial approval (as opposed to the Governor in Council).
Consultations pertaining to Food Marketing Authorizations are available under the Food and Nutrition "Public engagement and partnerships" page of the Health Canada website.
The ability to issue Interim Marketing Authorizations (IMA) has been replaced at the level of the Food and Drugs Act with the MA authority. As such, Health Canada will no longer be issuing IMAs. IMAs in effect prior to the coming into force of the new MA authority will continue until: a) the IMA is cancelled, b) the IMA becomes part of an MA, or c) two years after the day on which the IMA came into effect elapses. Health Canada is currently developing new approaches to implement food safety and nutrition decisions previously authorized on an interim basis through IMAs while regulatory amendments are being finalized.
The MA authority does not change Health Canada's ability to issue Temporary Marketing Authorization Letters (TMAL) where appropriate. Further information on TMALs is available in the document General Guidance Document for Temporary Marketing Authorization for Foods.
The table below provides links to Health Canada's current food-related MAs and any documents that are incorporated by reference into each MA.