PROGRAM SCHEDULED for November 17-20, 2014 | Paris, France
Your First and
Last Stop for
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 program 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.
- 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 programs, 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 Program.
- Attendees may apply for NY or NJ CLE credit
Please note that the Program tuition does not include hotel accommodations.
COST & REGISTRATION
Tuition for the Program: €3,500 (early-bird rate: €3,000 until September 16, 2014).
To request more information regarding the European Healthcare Compliance Certification Program, please click here to submit a 'Request for Information' form. You may also contact us at firstname.lastname@example.org or call 973-642-8871.