What is the FDA equivalent in Canada?

The Food and Drug Administration (FDA) and Health Canada are the regulatory authorities for USA & Canada respectively.

What is the Canadian equivalent of the FDA?

Health Canada is the federal body that regulates the drug approval process under the Food and Drugs Act (FDA) and its regulations (FDR), its related policies and guidance.

What is the difference between FDA and Health Canada?

Health Canada’s Health Products and Food Branch has a mandate of “minimizing health risk factors to Canadians while maximizing the safety provided by the regulatory system for health products”. The FDA’s mandate is “protecting the public health by assuring that…

Is Canada regulated by the FDA?

Food in Canada must comply with a range of regulations to ensure our health and safety. … They exercise this mandate under the authority of the FDA, and its regulatory mandate is pursued under the FDR.

Who regulates drugs in Canada?

Health Canada’s HPFB is the national authority that regulates, evaluates and monitors the safety, efficacy, and quality of therapeutic and diagnostic products available to Canadians.

How are drugs reviewed in Canada?

Before any drug can be sold on the Canadian market, it must go through a stringent drug review process conducted by Health Canada’s Health Products and Food Branch (HPFB). On occasion, external experts are also called upon to assess a particular drug’s safety, efficacy and quality.

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Who is the head of the Public Health Agency of Canada?

Public Health Agency of Canada

Agency overview
Minister responsible Hon. Jean-Yves Duclos, Minister of Health
Agency executives Iain Stewart, President of the Public Health Agency of Canada Dr. Theresa Tam, Chief Public Health Officer Dr. Howard Njoo, Deputy Chief Public Health Officer
Parent department Health Canada

What is FDA in America?

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 nation’s food supply, cosmetics, and products that emit radiation.

Who approves drugs in USA?

The pharmaceutical market in the United States was expected to increase from $354bn in 2015 to $497bn by 2020. The FDA is the main regulatory body that handles drug approval in the United States.

What is the FDA equivalent in China?

The National Medical Products Administration (NMPA) is the Chinese agency for regulating drugs and medical devices (formerly the China Food and Drug Administration or CFDA). The predecessor to the NMPA was initially founded in 1998 to oversee drugs and medical devices.