Regulatory Consultant, Tuija Keinonen, has extensive experience in contract research business, its establishment and working with pharma industry. She has been working in CRO industry about 30 years and acted as CEO for 15 years (Medfiles Group) as well as clinical research director, quality director and has led contract manufacturing organization. She has held several positions of trust both in the private and public sector as well as board memberships. Tuija applies her expertise for clinical trials, regulatory affairs and outsourcing strategy.
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