European Healthcare Compliance Programme
PROGRAMME OVERVIEW
The pharmaceutical, biotech and medical device industries are increasingly facing a more challenging regulatory and enforcement landscape throughout Europe. This intensive, multi-day educational and training programme addresses the myriad of legal, regulatory and compliance issues faced by pharmaceutical, biotech and medical device manufacturers doing business in Europe.
WHO SHOULD ATTEND
Legal, regulatory and compliance professionals and advisors working within the European pharmaceutical, biotech and medical device industries.
COST & REGISTRATION
Tuition for the Programme: €3,000 for registration by April 2, 2012 and €3,500 after April 2, 2012. To Register, please visit the SciencesPo website at http://www.sciences-po.fr/spf/conferences/certificat_healthcare.php
PROGRAMME DETAILS
- International faculty include high-level government regulators, health and legal scholars, in-house and outside counsel, consultants and industry compliance professionals.
- Session topics include anti-corruption laws, third-party risk, European healthcare reimbursement and delivery programmes, anti-trust/competition law, development, advertising and promotion of drugs and devices, fraud investigations and the European enforcement landscape, OECD directives, industry codes, privacy laws and much more.
- Attendees will receive a joint certificate issued by Seton Hall Law School and SciencesPo upon completion of the Programme.
More Information:
For information regarding the programme, please contact simone.handler-hutchinson@shu.edu or call 973-642-8863.


