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U.S. Food and Drug Administration.
FDA Approval: What it means. FDA approval of a drug means that data on the drugs effects have been reviewed by CDER, and the drug is determined to provide benefits that outweigh its known and potential risks for the intended population.
Some products such as new drugs and complex medical devices must be proven safe and effective before companies can put them on the market. The agency also must approve new food additives before they can be used in foods.
Health Canada : Health Canada is responsible for protecting human and animal health and the safety of Canadas food supply.
The United States Food and Drug Administration (FDA or US FDA) is a federal agency of the Department of Health and Human Services.
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Health Canada is the agency that is equivalent to the USs FDA. They approve food, drugs, medical therapies and medical equipment in Canada.
The Food and Drug Administration (FDA) is responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nations food supply, cosmetics, and products that emit radiation.
FDA is an agency within the Department of Health and Human Services.

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