Safe drugs and medical devices
The BfArM sets the agenda on several different levels. It is responsible for licensing and improving the safety of drugs, detecting and evaluating the risks of medical devices, and monitoring legal traffic in narcotic drugs and precursors. In these areas it defines limits wherever necessary and gives the green light wherever possible.
The BfArM also curates progress: it uses technologies of the future, such as artificial intelligence, novel designs for clinical studies and the exponential increase in data volumes (“big data”), to fulfil its core remit as best it possibly can. While all the time acquiring experience of the new technologies – of their advantages and disadvantages. “Digitisation in particular offers enormous opportunities when it comes to developing new therapies and efficiently delivering healthcare”, says Broich. The BfArM gives impetus in this area, allowing innovations to enter into widespread use more quickly. For example: a new way of reimbursing manufacturers was created so that patients could be prescribed “digital healthcare applications” – also known as “apps on prescription”. Using its fast-track system, the BfArM was able for the first time to define a comprehensive requirements profile for such applications in healthcare provision. Within three months, the claims made by manufacturers about aspects such as safety, performance and medical quality can be checked.