The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) is responsible for preparing the Agency's opinions on applications submitted for marketing authorisation and on all questions concerning medicinal products for human use. The CHMP organizes regular trainings on Quality, Safety and Efficacy topics. Registration procedure to EMA training activities may take up to 3 weeks. Interested persons are invited to fill in the Declaration of Interest for EMA training activities and to return the original duly signed to Mrs. Cathrin Budnik.

For registration and any further information on EMA activities send your request to Mrs. Cathrin Budnik, Secretary to Spiros Vamvakas.

Mailing Adress:
EMEA, 7 Westferry Circus, Canary Wharf, London, E14 4HB, UK
Email: Cathrin.budnik@ema.eu.int
Website: www.ema.europa.eu/