The European Centre for Regulatory Affairs (EUCRAF) offers a wide range of training resources and activities: postgraduate master program, seminars, coaching events, workshops, annual meetings, in-house trainings and webinars in the field of drug regulatory affairs and biopharma.
Our core programme is the Postgraduate Master Program that consists of 10 unique seminars designed to impart understanding in the current development and regulatory affairs of medicinal products with main focus on biopharmaceuticals.
The EUCRAF’s Annual Biopharmaceuticals Meeting is a platform for regulatory affairs professional to get yearly update in the field of approval of biopharmaceuticals from agency representatives and pharma experts (NEXT ANNUAL MEETING: 5 - 6 February 2015!). Our highly engaging and interactive Workshops focus on case studies - offering you deeper insights into specific topics of interest.
Our Coaching Events utilize the most active training technique possible: you can benefit from speakers with first-hand experience, small groups, and interactive problem-solving discussions.
Interested in our programme but unable to travel to our site? You can benefit at any place in the world from our Webinars produced from most of our events. Interested in our programme but you prefer to organize an In-house Training session? We come to you with our event management capabilities and provide our regulatory affairs training services at your company: tailor made to your needs.