Welcome to BdFMHP in Aufkirchen,
near Munich.

We offer medical and scientific advice to pharmaceutical companies and manufacturers of substance-based medical devices, enabling you to successfully develop your medicinal products or medical devices and maintain their life cycles after marketing authorisation or a CE mark has been granted. We support you in all the steps along the way, from trend analysis through preclinical testing and clinical development, to market launch.

Sie können diese Inhalte nicht sehen? Dann haben Sie entweder Javascript deaktiviert oder verfügen nicht über den aktuellen Flashplayer. Laden Sie sich hier den aktuellen Flashplayer herunter.

  • Do you need a trend analysis, expert report or risk assessment? Or have you received a deficiency letter? We can offer assistance with all of these, including meta-analyses or resistance reports – to name but a few.
  • Are you planning preclinical or clinical studies and looking for scientific advice or someone who can assume responsibility for the design and also expertly manage such projects? We can help you write protocols and final reports, advise you on the selection of contractual partners and carry out audits (monitoring) at the study sites.
  • Would you like individual advice on questions of drug safety/pharmacovigilance from a trusted service provider? We can also help you here. We can evaluate individual cases as well as handle complex issues such as writing periodic safety reports, compiling risk management plans or supporting you in the establishment of your entire pharmacovigilance system. Literature searches can also be performed to address your specific questions.

We can offer all of the above, and a whole lot more. We appreciate the importance of your products and so they will be in very good hands.