European Center of Regulatory Affairs

EUCRAF

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
Workshop

Speakers of the 2nd Annual EUCRAF Workshop
EUCRAF is pleased to introduce the speakers of the 2nd annual EUCRAF Workshop
Special Offer - Seminar 4.1 & 4.2
Book Seminar 4.1 (Pharmaceutical development of biopharmaceuticals and particulars of the CMC dossier) together with 4.2 (Non-clinical and clinical development of biopharmaceuticals including biosimilars and the Module 4 and 5 requirements)and receive 20% discount!
Speakers of Seminar 4.2
EUCRAF is pleased to announce the names of the speakers of Seminar 4.2.




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.

Novartis Novartis

Authorities

EMA
European
Medicines
Agency 		EU/ EEA
National
Agencies 		FDA
US Food
and Drug
Administration 		swissmedic
Schweizerisches
Heilmittel
Institut

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Scientific Course Commitee
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