Sabrina Stöhr

Merck Healthcare KGaA

Sabrina is a Regulatory Medical Writer with 10+ years of experience in clinical development. She has been involved in document writing across all stages of development and in various indications (e.g. oncology, inflammatory diseases, biosimilars). She has experience in the development of Briefing Documents directed to the EMA and FDA as well as other regulatory interaction and meetings. Following a PhD in human genetics and a postdoc in cancer research, she pursued an advanced training in clinical research before joining the pharmaceutical industry. Sabrina is also an experienced EMWA workshop leader.