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  • Precon I: Compliance 101
  • Precon II: Auditing and Monitoring Boot Camp
  • Precon III: A Comprehensive Overview of Pharma and Medical Device Corporate Integrity Agreements (CIAs)
  • Precon IV: The New Era of Scrutiny: FCPA Compliance in Pharma Operations
  • OIG Update
  • DOJ Criminal Division Update
  • Prosecuting Pharma and Device Fraud
  • FDA-DDMAC Update
  • AUSA Panel
  • Qui Tam Panel
  • State Enforcement Panel
  • Best Practices in Negotiating and Implementing CIAs
  • State Disclosure, Federal Sunshine Act and Global Transparency
  • Life Sciences in America the Morning after the Election
  • Managing Internal and External Investigations
  • PhRMA’s New Compliance Work Group Update
  • Global Pharma and Device Compliance Issues and Strategies

  • Mini Summit I: Co-pay Coupon Litigation Update
  • Mini Summit II: What Enhanced Obligations in CIAs and DPAs say about Agency Expectations for Compliance Programs
  • Mini Summit III: Compliance Issues in Global R&D and Medical Affairs
  • Mini Summit IV: US Disclosure Implementation Update
  • Mini Summit V: Medical Device Compliance Issues Update
  • Mini Summit VI: Global Pharma and Device Compliance Issues
  • Mini Summit VII: Anticorruption, Including FCPA and UK Bribery Act Update
  • Mini Summit VIII: Fair Market Value Update
  • Mini Summit IX: Enforcement Threat Against Individuals
  • Mini Summit X: Global Transparency Update
  • Mini Summit XI: Special Compliance Issues and of Small Pharma and Medical Device Companies
  • Mini Summit XII: Integrating a Culture of Ethics into Your Compliance Program
  • Mini Summit XIII: Government Price Reporting Update
  • Mini Summit XIV: Clinical Trial Disclosure and Results Reporting Liability under FDAAA, Section 801
  • Mini Summit XV: Board and Management Certifications and Working with an IRO
  • Mini Summit XVI: Drug Samples Disclosure: The Next Horizon?
  • Mini Summit XVII: Professional Responsibilities for Compliance Officers and In-house Counsel in the Pharmaceutical, Biotech and Medical Device Industries
  • Mini Summit XVIII: Compliance Program Innovation

Who Should Attend
  • Pharmaceutical and Health Care Executives and Board Members
  • Compliance Executives
  • Health Plan, Health System and Physician Organizations
  • Medical Directors
  • Physicians
  • Pharmacists and Pharmacy Technicians
  • Purchasers, including Private Employers and Public Purchasers
  • Pharmaceutical Manufacturers
  • Generic Pharmaceutical Manufacturers
  • Site Management Organizations
  • Clinical Research Organizations
  • Pharmacy Benefit Management Companies
  • Nurses
  • Health Plans and Health Insurers
  • Wholesale, Retail, Mail Order and Internet Pharmacies
  • Health Care Attorneys and In-house Counsel
  • Compliance Officers
  • Privacy Officers
  • Ethics Officers
  • Food and Drug Law Attorneys
  • Pharmaceutical Consultants
  • Investment Bankers
  • Venture Capitalists
  • Health Care Regulators and Policy Makers
  • Health Services Researchers and Academics
  • Auditors
About the Pharmaceutical Compliance Forum

The Pharmaceutical Compliance Forum (PCF) is a coalition of senior compliance professionals and legal counsel from more than 50 of the largest research-based pharmaceutical manufacturers. The PCF was founded in early-1999 by compliance professionals from the pharmaceutical industry to promote effective corporate compliance programs. The members meet twice a year, for two days, focusing on open and informal sharing of compliance information, best practices, and current developments in the field, and sponsors a three-day compliance congress each Fall. For membership information, contact Tim Bower at 215-599-6617 or via email at info@PharmaComplianceForum.org. Please visit their website at www.PharmaComplianceForum.org.

Overview | Agenda | Promotional Opportunities | Sponsors & Exhibitors
Speaking Proposals | Administration | Webcast Log In | Past Conferences | Contact Us | Home

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