Pharmaceutical law regulates the clinical testing, production and distribution of medicinal products. In addition to the relevant Medicines Act (AMG), additional subsidiary laws and regulations must be taken into account. Likewise, the European law level plays an important role. Not only for pharmaceutical companies, but also for the general practitioner often quite complicated legal issues arise in this context, which require legal clarification. We’re here to help!
You have changed the viewport. The page will be reloaded now. Please be patient.
