EUCRAF offers a wide range of training resources and activities: postgraduate programme, seminars, coaching events, workshops, annual meetings, in-house trainings and webinars in the field of drug regulatory affairs and biopharma.
The postgraduate programme 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. As of September 2015, the 6th turn, EUCRAF will offer a post graduate Certificate as “Regulatory Affairs Manager” based on 6 seminars. This allows you to tailor-made the programme to your specific needs.
The Annual Biopharmaceuticals Meeting is a platform for regulatory affairs professional to get yearly update in the field of approval of biopharmaceuticals.
Our Workshops focus on case studies and our Coaching sessions utilize the most active training technique possible: learn from speakers with first-hand experience, small groups, and problem-solving discussions.
You can also benefit at any place in the world from our Webinars produced from our events. With our In-house Training session, we come to you and provide our regulatory affairs training services at your company - tailor made to your needs.