Mr. Davidsenis an Associate in the Health Care and Life Sciences practice, in the Chicago office of Epstein Becker Green.
Advises clients on the research, development, and approval of pharmaceuticals, biologics, and medical devices
Develops clinical trial agreements, vendor agreements, informed consent documents, and related materials for clinical research sponsors, and negotiates agreements with clinical research institutions and investigators and with providers of clinical trial services
Counsels clients on fraud and abuse issues associated with pharmaceutical and medical device development and marketing activities
Prior to joining Epstein Becker Green, Mr. Davidsen was responsible for clinical trial outsourcing arrangements at an international pharmaceutical company specializing in hematology, oncology, and immunology. He served in a strategic management role with oversight on contract, budget, and informed consent development, review, and maintenance for more than 30 clinical trials for several oncology franchises before, during, and after FDA approval. He began his health care career negotiating clinical trial agreements at one of the largest pharmaceutical companies in the world to support cardiovascular, neurological, pediatric, and oncology studies.
Articles in the National Law Review database by Bradley S. Davidsen