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 composed of representatives of Health Authorities, EDQM, Universities Freiburg and Strasbourg, and of pharmaceutical companies.
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Application
Seminar 1 of the next course starts in September 2010. Flexible entry is possible, i.e. you can start the course any time. An Early Bird rate applies provided the application is sent five months in advance to the start Seminar desired!
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Book single Seminars
Biopharmaceuticals are special! Continue your training and book the single Seminars here.
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News
Attendees of first course
Speakers of Seminar 1
Career Prospects
Health authorities, institutions and companies which authorize, regulate, develop and market biopharmaceutcials present their organizations and departments here where professionals with interest in a career in regulatory affairs can work.
Authorities
| EMEA European Medicines Agency |
EU/ EEA National Agencies |
FDA US Food and Drug Administration |
swissmedic Schweizerisches Heilmittel Institut |
