Satu Kujala

Biography

 Satu Kujala has been with Medfiles since 1999. She worked as a clinical research director until 2006 and then as a regulatory affairs director until June 2014 when she was appointed the director of healthcare services. Currently, she is in charge of Medfiles’ clinical, regulatory, pharmacovigilance, and health economic services. She has worked for over 20 years in pharma industry and has gathered experience in clinical trials, regulatory affairs, price and reimbursement applications, pharmacovigilance, quality, and marketing. Satu Kujala has acted as the QPPV for Oy Medfiles Ltd since 2007 and also for several companies. She has also worked as a responsible director of the wholesale for several companies and as a QA responsible for an ISO9000 certified company. Her experience in clinical studies covers 12 years as a CRA, project manager, and research director with various duties ranging from study planning to writing of a final study report. She has also been a lecturer at the University of Helsinki and worked in a pharmacy. Satu Kujala has a broad knowledge of drug development and life-cycle management as well as a long track record in CRO business with wide range of duties from those of a scientific expert to marketing and business unit management

Research Interest

 drug developement and life cycle management