EUDRAC is a European specialised regulatory affairs and pharmacovigilance consultancy company providing support to drive products through development, registration, market launch and post-approval activities across all EU countries.
EUDRAC is based in Germany, France 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 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.