:
Breakout Sessions
:
Global Biotechnology Issues
:
Wednesday May 5, 2010
:
8:00 AM - 9:30 AM
:
McCormick Place, Chicago
:
S403B
:
Drug counterfeiting is as dangerous to patients as it is damaging to profits—and the market is only growing. It is estimated that within the next 18 months, counterfeit drugs will hold 14 percent of the total market, creating its own $75 billion industry. Biotech is not immune. By gaining key perspectives from stakeholders, we will discuss the relevance of anti-counterfeiting to the biotech community from early-stage to established biotechs, and practical options to respond to the threat. As we move toward health care reform, there is a need for increased communication and collaboration to find affordable and workable solutions. Panelists will discuss the challenges, opportunities and responsibilities from different viewpoints, highlighting key issues to be addressed by the industry.
Program: Hot Topic
:
1. Understanding the commercial impact of counterfeiting, in terms of revenue, brand protection and acquisition value
2. Outline different approaches to address the challenges of integrating strategic, low-cost authentication technologies.
3. “Bridging the gap” between early-stage and big biotech – where in the development cycle to address counterfeiting issues
Pamela McNamara - Chair
President
Cambridge Consultants
Lew Kontnik, JD
Director, Brand Protection
Amgen Inc
Hugh Burchett, PhD
Director, Defence and Security Business
Cambridge Consultants Ltd
Dave Kent, MS,BS
Vice President of Global Risk
Genzyme Corporation
Andrew Emmett, MPH
Director, Science & Regulatory Affairs
Biotechnology Industry Organization