by sdran | Dec 23, 2021 | OUS-Regulatory: Other National Reg. Agencies & international Res.
The International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) is a unique project that brings together the regulatory authorities of Europe, Japan and the United States and experts from the...
by sdran | Dec 23, 2021 | OUS-Regulatory: Other National Reg. Agencies & international Res.
The MHRA is an executive agency of the Department of Health of UK which is responsible for ensuring that medicines and medical devices work, and are acceptably safe. VISIT SITE
by sdran | Dec 23, 2021 | OUS-Regulatory: Other National Reg. Agencies & international Res.
European Medicines Agency (EMA) is a decentralized body of the European Union with headquarters in London. Its main responsibility is the protection and promotion of public and animal health, through the evaluation and supervision of medicines for human and veterinary...
by sdran | Dec 23, 2021 | OUS-Regulatory: Other National Reg. Agencies & international Res.
Health Canada’s Therapeutic Products Directorate is the Canadian federal authority that regulates pharmaceutical drugs and medical devices for human use. Prior to being given market authorization, a manufacturer must present substantive scientific evidence of a...
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