Keynote Speakers:Dara Corrigan, FDAVincente Rodriguez Fuentes, Abogado, Legal Agrifood AbogadosFlora Okereke, Head of Regulatory Policy, British American TobaccoJim Solyst, Director of Government Affairs, Swedish MatchCarmen M. Shepard, Senior Vice President, Global Policy and Regulatory Counsel, Mylan Inc. Nicole Coutrelis, Avocat au Barreau de Paris, COUTRELIS & ASSOCIESLuis Perez, CFE, Senior Operations Manager, Office of Criminal Investigations, FDA; Intellectual Rights Property Center Liaison for FDA/OCIJohn L. Robertson, Supervisory Special Agent, Intellectual Property Rights Liaison, Federal Bureau of InvestigationMinnie Baylor-Henry, Worldwide Vice President for Regulatory Affairs, Johnson & JohnsonCharles Hamshaw-Thomas, Director, Legal and Corporate Affairs, E-LitesGeoffrey M. Levitt, Senior Vice President and Associate General Counsel, Regulatory & Policy, PfizerAnd more!Agenda Highlights:Tobacco: Potential Reduced-Risk Products – an Examination of New Products and RegulationsDrugs and Devices: Quality Control Issues in the US and EUFood: Food Labeling and Health ClaimsCounterfeitingInternet Sales: Regulations and RisksAdvertising and Promotion: What Can You Really Say about Your Product?Trade Treaties & Importation: What You Need to Know About the TTIPEmerging Issues You May Not Have Considered — The Global PerspectiveWhy Attend:This landmark two-day conference in Brussels, Belgium provides an unparalleled opportunity to hear directly from internationally renowned experts on game-changing developments and analytical comparisons in food, medical device, drug and tobacco regulation and policy in Europe and the United States. FDLI has invited officials from FDA, EMA and the EU, top officials of multi-national manufacturers and seasoned legal experts to provide practical advice on the similarities and difference in regulatory schemes. Attendees will have a unique opportunity to build their global professional network, strengthen existing partnerships and better prepare their businesses for upcoming changes in regulations and policy on both sides of the pond.Who Should Attend:Representatives of European/U.S. food, tobacco, pharmaceutical and medical device companies or those who wish to partner with these companies Food and Drug AttorneysGovernment OfficialsAcademicsFood and Drug Industry ConsultantsVenture Capitalists and Investment Brokers doing business in the EU and US