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Federal Institute For Drugs And Medical Devices

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Federal Institute for Drugs and Medical Devices The BfArM is a Federal ...

Bundesinstitut für Arzneimittel und Medizinprodukte

Emer Cooke, Director of the European Medicines Agency (EMA), and Prof. Dr. Karl Broich, President of the Federal Institute for Drugs and Medical Devices (BfArM), talk about their current cooperation and their ideas for the future.

The BfArM provides an overview of the most relevant European and national regulations for Medical Devices and the national laws for digital applications. This is not an exhaustive

The Federal Institute for Drugs and Medical Devices is located in the federal quarter of Bonn near junction („Autobahn-Anschlusstelle“) Bonn-Rheinaue (A 562) and the sub-way station Robert

Field Corrective Actions include removals of medical devices from the market or any other corrective action on devices in use. In general, the manufacturer implements field corrective

Emer Cooke, Director of the European Medicines Agency (EMA), and Prof. Dr. Karl Broich, President of the Federal Institute for Drugs and Medical Devices (BfArM), talk about their

The Federal Institute for Drugs and Medical Devices (BfArM) is a higher federal authority within the portfolio of the Federal Ministry of Health. BfArM’s responsibilities include the approval of drugs for the treatment of humans as

Federal Institute for Drugs and Medical Devices

Federal Institute for Drugs and Medical Devices Address Kurt-Georg-Kiesinger-Allee 3 53175 Bonn Country Germany Phone +49 228-207-30 Fax +49 228-207-5207 Email

In according with the Act on Medical Devices (MPG) and the German Safety Plan for Medical Devices (MPSV), the Federal Institute for Drugs and Medical Devices (BfArM) ensures 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

Performance studies of in vitro diagnostic medical devices. To overview: Performance studies of in vitro diagnostic medical devices; Halt, Termination or End of a Performance Study ; Request

A network for health in Europe. Emer Cooke, Director of the European Medicines Agency (EMA), and Prof. Dr. Karl Broich, President of the Federal Institute for Drugs and Medical Devices

The Federal Institute for Drugs and Medical Devices (in German “Bundesinstitut für Arzneimittel und Medizinprodukte, BfArM”) is a central authority of the German healthcare system and

We are experiencing a previously unknown dynamic in the network

The Paul-Ehrlich-Institut, Federal Institute for Vaccines and Biomedicines, makes an essential contribution to the availability and safety of effective biomedical products. The regulatory

BfArM Recommendations include information about risks arising from medical devices and measures recommended by the Federal Institute in order to reduce or eliminate risks. The

Tasks. The Federal Institute for Drugs and Medical Devices (BfArM) provides an overview of current supply shortages for medicines for human use (excluding vaccines) in Germany.The

Basically, according to § 8 of the Medical Device Operator Ordinance (MPBetreibV), proper reprocessing is presumed if the recommendation of the Robert Koch Institute and the BfArM on

Compassionate use notifications should be submitted in paper and CD-ROM/DVD to the following address:. Federal Institute for Drugs and Medical Devices (BfArM) Clinical Trials/GCP Kurt

The information on medicinal products provides the drug information system of the competent authorities BfArM (Federal Institute for Drugs and Medical Devices), PEI (Paul-Ehrlich-Institut)

The information on medicinal products provides the drug information system of the competent authorities BfArM (Federal Institute for Drugs and Medical Devices), PEI (Paul-Ehrlich-Institut)

Direct Healthcare Professional Communication (DHPC) on Livopan (Nitrous Oxide/Oxygen) 50 %/50 % gas for medical use, compressed: Risk of gas leakage and

As an independent higher federal authority of the Federal Ministry of Health, the Federal Institute for Drugs and Medical Devices pursues the goal of maximizing drug and patient safety. Its

The RKI is the Federal Government’s central institution in the field of public health responsible for identifying, preventing and combating diseases and serves as the National Institute of Public

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 Rapid

The Federal Institute for Drugs and Medical Devices (Bundesinstitut für Arzneimittel und Medizinprodukte, BfArM) is an independent federal higher authority within the portfolio of the

In according with the Act on Medical Devices (MPG) and the German Safety Plan for Medical Devices (MPSV), the Federal Institute for Drugs and Medical Devices (BfArM) ensures the