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 certification in healthcare compliance 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.