View assessment reports for authorized medicinal products
Source: BUS Rheinland-PfalzIn the so-called public assessment reports (PAR), the Federal Institute for Drugs and Medical Devices (BfArM) informs users, for example
- Doctors,
- pharmacists and
- other healthcare professionals.
The PARs contain information on medicinal products and medical devices regarding
- quality,
- efficacy,
- safety or
- risks, such as areas of application and possible side effects.
The PARs are intended to contain all essential information for the authorization decision and are a supplement to the already publicly available information for healthcare professionals and package leaflets.
The assessment reports published by the BfArM refer to medicinal products for human use. They are published on the portal for medicinal product information of the federal and state governments (online platform PharmNet.Bund).
You can view these assessment reports there at any time.