Public Policy: Improving Public Health

Fostering innovative approaches to patient care that focus on delivering value and world-class outcomes to maximize resources and improve quality of life.

Around the world, illegitimate drugs, whether fake, falsified, or substandard, pose a significant threat to patients. While many think of illegitimate drugs as a problem unique to developing countries, over the last few years, the United States has seen numerous incidences of these illegitimate medications making their way into the legitimate supply chain and into the hands of patients. Over the last few weeks, both the House and Senate have demonstrated strong commitments to strengthening our supply chain and protecting patients through the development of national track-and-trace standards.

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In the Senate, Chairman Harkin, Ranking Member Alexander, and Senators Bennet and Burr submitted draft legislation to the Committee on Health, Education, and Pensions. In reference to the need for national track-and-trace standards, Senator Bennet remarked, “Over the past few years, we’ve had a record number of recalls and reports of tainted or ineffective drugs reaching our hospitals and drug store shelves. In fact, right now, we know more from a barcode on a gallon of milk than from a barcode on a bottle of pills, which could mean the difference between life and death.” This bipartisan move represents a promising step toward the kinds of standards necessary to ensure patients receive safe and effective medicines. However, the Senate isn’t the only side of Congress recognizing this critical need...

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My colleague, Femke Beumer, originally blogged on this topic for LillyPad E.U.

Last week, a delegation of ten Members of European Parliament gathered in Washington to lay down the political groundwork for the proposed EU-US trade deal. With formal negotiations kicking off in July, the delegation has already reported back saying that they find their US Congress counterparts in"an increasingly positive mood".

We're delighted to hear it. We've spoken before about our support for the agreement: if it bears fruit, the deal promises to improve the economic competitiveness of both partners, and more importantly, to help improve the health of patients everywhere. The prospect of what we could achieve if we have more convergence of our rules and standards is something that truly excites not just Lilly but the whole biopharmaceutical industry...

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Look out Chicago! Next week, LillyPad will be reporting from the 2013 BIO International Convention, the world’s largest gathering of biotechnology leaders. Every year, the BIO International Convention brings together industry leaders to address key issues and make vital connections needed to drive future innovations that can improve patient health and quality of life in all regions of the world.

This year represents the 20thanniversary of the BIO International Convention and I’ll be there ready to live up to this year’s theme: “Connect. Partner. Innovate.” With exhibits spanning the size of four football fields, and a program with over 125 sessions in 17 topic areas, it promises to be an exciting week. Over 800 speakers will share their expertise and insights on the breakthroughs in medicine, diagnostics, the environment, energy production, food and agriculture and more. This list of impressive individuals includes several of Lilly’s own employees, speaking on topics from trade to online advocacy (that’d be me!). In addition, Lilly will be hosting and sponsoring events throughout the week...

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Last week, Lilly’s Communication Manager for Global Health Programs, Karen Van der Westhuizen, wrote a terrific guest blog highlighting the need for public-private partnerships to tackle non-communicable diseases worldwide. Today, I wanted to take a look at another growing global health issue—counterfeit medications. What better way to explore the topic than with a quiz?

True or False: Counterfeit medications primarily affect the health of those in developing countries...

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Substandard and counterfeit medicines pose a significant threat to patients worldwide. The continuous and growing danger from criminal organizations producing these falsified and substandard drugs requires a coordinated response from policymakers. A report issued yesterday by the Institute of Medicine (IOM) underscored this point and demonstrated the urgent need for national and international action to improve the integrity of the pharmaceutical distribution supply chain.

Currently, the U.S. pharmaceutical distribution supply chain is subject to a patchwork of state laws, creating vulnerabilities easily exploited by counterfeiting networks...

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