FEDERAL INSTITUTE FOR DRUGS AND MEDICAL DEVICES
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 Federal Ministry of Health. At the BfArM, roughly 1,000 employees (physicians, pharmacists, chemists, biologists, lawyers, engineers, technical assistants, administrative staff etc.) are involved in the tasks of licensing, improving the safety of medicinal products, detecting and evaluating the risks of medical... devices, and monitoring the legal traffic in narcotic drugs and precursors. The most important aim of these activities is to increase the safety of medicinal products and thus that of the patients. Consequently, the BfArM makes a major contribution towards the prevention of risks to public health. The BfArM is located in Bonn. In the course of moving the government's seat from Bonn to Berlin, the Berlin/Bonn Act specified that the authority was to move from Berlin to Bonn as a compensation measure for the Federal City Bonn. Revenue and expenditure of the BfArM are described in Chapter 1510 of the Federal Budget; the sound budgetary management is monitored by the Federal Ministry of Health (Bundesministerium für Gesundheit, BMG) and the Federal Audit Office (Bundesrechnungshof). The revenue mainly results from fees charged for official acts. Additional revenues are from mandates assigned by the European Medicines Agency EMA and other healthcare institutions. The BfArM does not engage in any promotion and has no income based on advertising.
FEDERAL INSTITUTE FOR DRUGS AND MEDICAL DEVICES
Social Links:
Industry:
Education Government Health Care
Founded:
1994-01-01
Address:
Bonn, Nordrhein-Westfalen, Germany
Country:
Germany
Website Url:
http://www.bfarm.de
Total Employee:
11+
Status:
Active
Email Addresses:
[email protected]
Technology used in webpage:
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http://www.bfarm.de
- Host name: 80.245.152.209
- IP address: 80.245.152.209
- Location: Germany
- Latitude: 51.2993
- Longitude: 9.491
- Timezone: Europe/Berlin
More informations about "Federal Institute for Drugs and Medical Devices"
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Tasks. The authorisation of finished medicinal products on the basis of the Medicinal Products Act (Arzneimittelgesetz, AMG) is one of the main tasks of the BfArM.In the course of these …See details»
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Das BfArM stellt im Hinblick auf die Gewährleistung von Unabhängigkeit und Transparenz sicher, dass die mit der Zulassung und Überwachung befassten Mitarbeitenden keine finanziellen …See details»
Federal Institute for Drugs and Medical Devices (BfArM)
Federal Institute for Drugs and Medical Devices (BfArM) Better health for all citizens is the goal of the work of the Federal Centre for Health Education. As the higher authority specialised in …See details»
Federal Institute for Drugs and Medical Devices - Wikipedia
The Federal Institute for Drugs and Medical Devices is one of the two independent federal higher authorities in the German health care sector alongside the Paul-Ehrlich-Institut (PEI) under the Federal Ministry of Health. It is headquartered in Bonn, Germany. The core tasks of the BfArM as a regulatory authority include the approval and registration of medical devices and products, including drugs in the special therapeutic areas of herbalism and paraherbalsSee details»
Federal Institute for Drugs and Medical Devices
Aug 9, 2023 Various interdisciplinary researchers groups of BfArM work closely with leading national, European and international universities and non-university research institutions. International. As Europe’s largest medicines regulatory …See details»
Germany: Federal Institute for Drugs and Medical Devices (BfArM)
The Federal Institute for Drugs and Medical Devices (BfArM) is responsible for licensing and registering finished medicinal products as proof of safety and efficacy. BfArM monitors the …See details»
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BfArM as employer. The BfArM is the largest European body in the area of licensing and safety of drugs and medical devices. Around 1,300 employees in a wide range of disciplines are committed to the safe care of patients. Of the …See details»
BfArM Jahresbericht | A network for health in Europe
The extended mandate has not changed the basic system for regulating medicines in Europe. In it, the EMA, just like the BfArM, is a member of the network of the heads of the national competent authorities, abbreviated as …See details»
National competent authorities - European Medicines …
The European Medicines Agency works closely with the national competent authorities of the Member States of the European Union (EU) and the European Economic Area (EEA) responsible for medicinal products for human use.See details»
5. The institutions | IQWiG.de
BfArM also monitors the safety of drugs and medical devices. Since 2020, BfArM has also been evaluating some of the digital health applications of the low-risk classes I and IIa, and deciding on their inclusion in the catalogue of health …See details»
PharmNet.Bund - Drug information system
Research medicinal products - prices and conditions (BfArM website) Supporting information. The information on medicinal products provides the drug information system of the competent …See details»
BfArM - Medicinal products information
The BfArM does not receive any information on the reasoning for such a withdrawal and can therefore not publish any. The reference to the administrative finality is also not applicable. …See details»
BfArM - Geschichte
Dem BfArM werden für diese Überwachung des legalen Verkehrs mit diesen Stoffen zahlreiche Aufgaben übertragen. 1999. Erster Spatenstich für den Neubau des Instituts in Bonn. Das …See details»
BfArM office in Cologne - Homepage - DIMDI
Visit bfarm.de. To the article. Information for Professionals. Certificate of conformity. BfArM provides EU certificates of conformity and the Statement of Need. Read more (in German …See details»
BfArM Jahresbericht | Homepage | The BfArM in figures
How many medicinal products are marketable in Germany? How many clinical trials are registered each year? How many risk reports for medical devices are received by the BfArM? This …See details»
Federal Institute for Drugs and Medical Devices - Crunchbase
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 …See details»
BfArM - Medical devices
The tasks of BfArM in the field of medical devices result in particular from the Medical Device Regulation (MDR) (EU) 2017/745, the Medical Device Law Implementation Act, the …See details»
BfArM - Impulse Report 2023 - jahresbericht.bfarm.de
If unwanted side-effects arise in a drug, mechanisms are put in place at an EU level to minimise risks. The BfArM brings its expertise to the committees of the European Medicines Agency …See details»
BfArM - Medicinal products
The notification can preferably be made electronically to [email protected] or by postal mail to Unit 75 of the Federal Institute for Drugs and Medical Devices. The notification of the …See details»
BfArM - EU and International
International collaborations promote networking and exchange between BfArM and public health actors, and contribute to global health protection. The executive department coordinates the …See details»