Birgitta K Grundmark is an Oncologist and Clinical Pharmacologist with over 20 years of experience in Pharmacovigilance at both European and global levels. Currently serving as Safety Physician Sr PhV Expert at PharmaRelations and as a member of the ISoP Scientific Board, Grundmark has held several key positions including Senior Clinical and Pharmacovigilance Advisor at the Norwegian Medicines Agency and Sr PhV Expert at Uppsala Monitoring Centre. Additional expertise includes roles as Independent PhV Expert to the PRAC at the EMA/EU Commission and Risk Management Specialist at the European Medicines Agency. Grundmark's background encompasses significant contributions to signal detection, management methods development, and education in global pharmacovigilance, supported by a Doctor of Medicine degree from Uppsala University.
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