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The Food and Drugs Act (French: Loi sur les aliments et drogues) is an act of the Parliament of Canada regarding the production, import, export, transport across provinces and sale of food, drugs, contraceptive devices and cosmetics (including personal cleaning products such as soap and toothpaste). It was first passed in 1920 and most recently ...
Canada's drug regulations are measures of the Food and Drug Act and the Controlled Drugs and Substances Act.In relation to controlled and restricted drug products, the Controlled Drugs and Substances Act establishes eight schedules of drugs and new penalties for the possession, trafficking, exportation and production of controlled substances as defined by the Governor-in-Council.
The Controlled Drugs and Substances Act (French: Loi réglementant certaines drogues et autres substances) is Canada's federal drug control statute. Passed in 1996 under Prime Minister Jean Chrétien's government, it repeals the Narcotic Control Act and Parts III and IV of the Food and Drugs Act, and establishes eight Schedules of controlled substances and two Classes of precursors.
The Food and Drugs Act does not provide the power to recall food products and all recalls are done on a voluntary basis. However, Section 19 of the Canadian Food Inspection Agency Act provides authority for the Minister of Agriculture to order a recall, where there are reasonable grounds that the product poses a risk to public, animal or plant ...
Dominion Elections Act, 1920; Food and Drugs Act, 1920; Canadian Nationals Act 1921; ... Canadian Football Act 1974; 1980 – 1989. Tax Court of Canada Act, 1980;
What is listed in Canada's set of Food and Drug Regulations [5] The name prescribed by another federal regulation; The name by which the food is formally known (for example: orange juice) The name of the product must also be displayed on the main label in both English and French with a minimum height of 1/16 of an inch (1.6 mm). [6]
Pages in category "Canadian food law" The following 12 pages are in this category, out of 12 total. ... Food and Drugs Act; H. Canadian health claims for food;
The EUND pathway was developed to allow a mechanism for authorization of these drugs based on non-clinical and limited clinical information. A manufacturer of a new drug may file an extraordinary use new drug submission for the new drug if, under paragraph C.08.002.01(1): [2] (a) the new drug is intended for