EUDRAC
Regina Jakob is a seasoned professional in regulatory affairs and pharmacology with extensive experience spanning over two decades. Currently serving as a Senior Regulatory Affairs Consultant at EUDRAC since February 2020, Regina has a proven track record of obtaining marketing authorization for pharmaceuticals in Germany, including generics, and managing EU procedures and submissions. Previously, Regina held the position of Regulatory Affairs Manager at PharmaLex GmbH and Pharma Resources GmbH, where responsibilities included project management and submissions at both national and EU levels. Academic roles include lectureships at Martin-Luther-Universität Halle-Wittenberg and Humboldt University of Berlin, as well as research associate positions at prestigious institutions such as the University of Pittsburgh, University of Rochester Medical Center, and the University of Chicago. Regina holds a Ph.D. in Pharmacology and a state diploma in Pharmacy from The Philipp University of Marburg.
This person is not in any teams
EUDRAC
EUDRAC is a European specialised regulatory affairs and pharmacovigilance consultancy company providing support to our clients to drive products through development, registration, market launch and post-approval activities across all EU countries. EUDRAC is based in Germany, France, Switzerland and the UK, successfully guiding pharmaceutical and medical device companies since 2002. Our expertise covers a wide spectrum of therapeutic areas and pharmaceutical forms. Our experienced staff (majority have more than 10 years of experience) includes pharmacists, chemists, biologists, a medical doctor, and pharmacovigilance and regulatory affairs specialists. A high level of repeat business and ongoing long–term assignments with our clients is proof of our excellent service. We are dedicated to provide “quality for success” for your projects. Let us help you to achieve your goals!