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 risks of medicinal products by collecting and evaluating laboratory reports. The institute also evaluates and develops safe medical devices in Germany. The BfArM site contains information about the institute and its functions, medicinal products, and medical devices. Various research documents covering topics such as pharmacogenomics, pharmacoepidemiology, safety of medical devices, neuropsychopharmacology, special indications, and biostatistics are also available.