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International Federation of Pharmaceutical Manufacturers & Associations UNODC Conference on Fraudulent Medicines William S. Reid Senior Director, Global Anti-Counterfeiting Operations Eli Lilly and Company 15 February 2013

Ifpma william reid_unodc_conference on fraudulent medicines_15_feb2013

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IFPMA presentation, UNODC, Technical Conference on the Trafficking in Fraudulent Medicines, William S. Reid, Senior Director, Global Anti-Counterfeiting Operations Eli Lilly and Company (Vienna, 15 Feb 2013)

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International Federation of Pharmaceutical Manufacturers & Associations

UNODC Conference on Fraudulent Medicines William S. Reid Senior Director, Global Anti-Counterfeiting Operations Eli Lilly and Company 15 February 2013

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Outline

1. Our engagement

2. Current challenges in fighting counterfeit medicines

3. Case studies

4. Conclusions

15 February 2013 © IFPMA 2013 2

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Our Engagement

• Anti-counterfeiting is an industry priority IFPMA Ten Principles Partnerships Policy research Awareness raising

• Support to WHO initiatives

15 February 2013 © IFPMA 2012 3

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Our Ten Principles

15 February 2013 © IFPMA 2012 4

• Medicine counterfeiting is first and foremost a crime against patients

• Counterfeit medicines threaten the full spectrum of legitimate medicines

• Patents have nothing to do with counterfeiting and counterfeiting has nothing to do with patents

• Global cooperation is needed

• WHO leadership is critical

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Position on Internet

Sales and Access to

Safe Medicines

UCL policy report:

Falsified medicines and global

public’s health

FIP-IFPMA Document:

The threat of false friends

Workshop: The threat of false friends Fake medicine - Imminent Risks to Global Health

Our Recent Initiatives

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Current Challenges

a. Detection of counterfeit medicines requires control of supply chain and enhanced regulatory capacity

b. Lack of global data and health impact assessment require regular reporting from competent authorities and other organizations

c. Robust and adapted legislative and regulatory

frameworks require continuous enforcement efforts at national and international level

15 February 2013 © IFPMA 2013 6

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Case Studies

a. Scope: global, multiple therapeutic areas, patented and generic medicines

b. Illegitimate Internet sales c. Unregulated API d. Legislative challenges: Jurisdictional alignment,

statutory limitations, domestic resource constraints e. Opportunities: New technology & tools, growing

awareness and actions, shared commitment to patient safety

15 February 2013 © IFPMA 2012 7

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Conclusions

Robust Regulatory Framework

and Enforcement

Education and

Awareness Raising

Capacity Building

International multi-sector Cooperation

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Thank you

15 February 2013 © IFPMA 2012 9