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 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!
Our highly qualified and experienced management team each have more than 25 years experience in regulatory affairs. Please see more information about our management team, below.