Programme
International Seminar Programme "Regulatory Affairs for Biopharmaceuticals including ATMPs" (Seminars and Postgraduate Master Programme)
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Organisation
EUCRAF and its SCIENTIFIC COURSE COMMITTEE is composed of representatives of Health Authorities, EDQM, Universities Freiburg and Strasbourg, and of pharmaceutical companies.
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MSc-Course
The full course takes one year and can be started at any time. The course is attended by students who start their career as graduates from different universities, from companies like Novartis, Xendo, Merck Serono and Authorities such as PEI.
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Seminars
Biopharmaceuticals are special! Continue your training and book the single Seminars here.
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News
Photos of Seminar 5
Speakers of Seminar 6
Speakers of the Immunogenicity Integrated Workshop 2012
Workshops
Career Prospects
Health authorities, institutions and companies which authorize, regulate, develop and market biopharmaceuticals present their organizations and departments here where professionals with interest in a career in regulatory affairs can work.
Authorities
| EMA European Medicines Agency |
EU/ EEA National Agencies |
FDA US Food and Drug Administration |
swissmedic Schweizerisches Heilmittel Institut |
