255584 Searching for better global health governance for dangerous counterfeit medicines

Wednesday, October 31, 2012 : 8:30 AM - 8:50 AM

Timothy Mackey, MAS , School of Public Health (SDSU), Institute of Health Law Studies (Cal Western School of Law), San Diego State University-University of California, San Diego and Institute of Health Law Studies, Cal Western School of Law, San Diego, CA
Bryan Liang, MD, JD, PhD , School of Medicine (UCSD), Institute of Health Law Studies (Cal Western School of Law), University of California, San Diego, California Western School of Law, San Diego, CA
Perhaps no greater challenge exists for global health security and patient safety than fake, unregulated, and/or poor quality drugs, collectively “dangerous counterfeit medicines” now endemic in the global drug supply chain. Dangerous counterfeit medicines are prevalent everywhere including traditional healthcare settings, pharmacies, and the Internet. These dangerous medicines are on the rise in both therapeutic and geographic scope, threatening patient lives, potentially leading to antimicrobial resistance, and profiting illicit actors. Yet, despite these clear threats, surveillance is extremely limited, with available data pointing to an exploding global health crisis worldwide. Data from the Pharmaceutical Security Institute (“PSI”), indicates an alarming global increase in total incidents of counterfeiting in all global regions and for a wide range of medical products. Efforts such as World Health Organization IMPACT have made inroads in combating this illicit trade, but are stymied by ineffectual governance and conflict between ideologies of access to medicines and intellectual property rights. To address this important issue we advocate for the establishment of a comprehensive global health governance framework leveraging the respective strengths of international organizations. This includes utilizing the United Nations Office on Drugs and Crime (“UNODC”) for global enforcement against dangerous counterfeit medicines and focusing the World Health Organization's efforts on providing technical assistance on surveillance and collecting epidemiological data on dangerous counterfeit medicines as well as developing programs to improve access to safe medicines.

Learning Areas:
Public health or related laws, regulations, standards, or guidelines
Public health or related public policy

Learning Objectives:
• Describe continuing growing global crisis of dangerous counterfeit medicines and data indicating global increase in incidents of drug counterfeiting. • Assess current limitations of global health governance framework addressing dangerous counterfeit medicines including debate over access to medicines and intellectual property and failure to coordinate global action. • Formulate a policy proposal that advocates for better utilization of respective strengths and expertise of international organizations such as UNODC, WHO, and Interpol to address this crucial global health problem.

Keywords: Policy/Policy Development, Public Health Policy

Presenting author's disclosure statement:
Organization/institution whose products or services will be discussed: none

Qualified on the content I am responsible for because: I hold a masters degree in health law and am a current PhD student in global health. I am a co-author on several peer-review manuscripts on global health policy and have also given oral presentations at several international and domestic public health conferences including APHA.
Any relevant financial relationships? No

I agree to comply with the American Public Health Association Conflict of Interest and Commercial Support Guidelines, and to disclose to the participants any off-label or experimental uses of a commercial product or service discussed in my presentation.