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Clinical trials are performed before the product concerned is placed on the market and they have to be approved in Germany by the respective competent federal higher authority.
15 thg 11, 2024 · The FDA Europe's Office mission is to strengthen the safety, quality, and effectiveness of medical products and food produced in Europe for export to the United States.
The Federal Institute for Drugs and Medical Devices (in German: Bundesinstitut für Arzneimittel und Medizinprodukte – BfArM) is the medical regulatory body in Germany.
Digital applications are an important element in the digital modernisation of health care and nursing in Germany. They are part of the future eHealth infrastructure and will interact closely …
AIDS education is one of the central tasks of the Federal Centre. The campaign “Don’t give AIDS a chance”, launched in 1987, is the largest and most comprehensive campaign mounted by …
19 thg 8, 2025 · Below you will find all important information about the changes in the radiation protection act applicable since 01.07.2025. Here the BfArM publishes the current processing …
15 thg 7, 2025 · The Federal Institute for Drugs and Medical Devices (BfArM) is an independent federal higher authority within the portfolio of the Federal Ministry of Health (BMG) with the …
PharmNet.Bund.de is a cooperative project of the German regulatory authorities – Federal Institute for Drugs and Medical Devices (BfArM), the Paul-Ehrlich-Institut (PEI) and the Federal …
The Federal Institute for Drugs and Medical Devices (BfArM) provides an overview of current supply shortages for human medicinal products (excluding vaccines) in Germany.
The United States Food and Drug Administration (“U.S. FDA”) and the German Federal Institute for Risk Assessment (Bundesinstitut für Risikobewertung, hereinafter “BfR”), collectively ...
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