Dr. Joan D’souza is a senior pharmacovigilance and regulatory affairs professional with extensive global experience across the US and Europe. Currently serving as Fachtechnisch verantwortliche Person (FvP) (Responsible Person), Local Qualified Person for Pharmacovigilance (LQPPV) and Regulatory Affairs (LCPRA) in Switzerland, Germany, and Liechtenstein—as well as Deputy LCPPV in the UK and Ireland and Pharmacovigilance Physician—she oversees comprehensive safety surveillance and regulatory compliance across the entire product lifecycle, from market release decision to submission.
With a rare combination of qualifications—a medical degree, licensure as a U.S. attorney, a Master’s in Pharmacovigilance, and ongoing PhD studies through the Pharmacy department in University of Strassbourg (France)—Joan brings a uniquely multidisciplinary perspective to drug safety and GxP quality assurance. Her work involves direct engagement with health authorities to ensure clinical compliance across clinical development and post-market activities.
As the founder of JD Pharma Services, a one-stop solution provider for pharmaceutical needs, and a moderator of the RA, PV, and Drug Device Combinations Working Groups at Zug Pharma Group, as well as former President of the ISoP Swiss and Austria Chapter, Joan remains a driving force in safety, regulatory intelligence, vendor oversight, and pharmacovigilance training. Fluent in English and German, she is dedicated to advancing patient safety through operational excellence and regulatory integrity.