Eucraf Workshop "Immunogenicity integrated"

interactive workshop to apply risk assessment tools in parctice

Munich, October 15 - 16, 2012

15% discount on registration fee for EAPB members - mention "EAPB member" on the registration form.

Current regulatory environment, including biosimilars
Mechanisms involved in immune responses to therapeutic proteins
Bioanalytical method selection for immunogenicity testing
Identification of product-specific risk factors
Multi-disciplinary evaluation of risks
Integrated data interpretation
Interactive expert panel discussions & case study

further information with details for registration, location and programme you find on Eucraf's website
flyer
registration form

Contact person: Anita Dioszegi, Programme Manager
E-mail: anita.dioszegi@eucraf.eu / Phone: +49 761 1373 4424

Study Director: Dr. Gabriele Dallmann, Study Director
E-mail: gabriele.dallmann@eucraf.eu

EUCRAF - the European Centre for Regulatory Affairs Freiburg offers in collaboration with the University of Strasbourg the postgraduate Diploma "Regulatory Affairs for Biopharmaceuticals" developed by distinguished experts from authorities, universities and companies. EUCRAF is also a platform for Regulatory Affairs experts to facilitate the exchange on current matters related to biopharmaceuticals.

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