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PPA strives to improve patient health, advance medical innovation and fuel economic growth.

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Patent protection should always be considered by an inventor during the initial stages of their invention.

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Many Americans are struggling to afford their medicines and have important questions about their medicine costs. Let's Talk About Cost addresses these questions.

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There are a lot of conversations in Washington about how to change Medicare Part D, but they aren't always focused on what seniors care about most: affordability and predictability.

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We are creating a place where we can share ideas, provide the perspective of America's biopharmaceutical companies and, most importantly, listen to you.
Sarah K. Martin

Sarah K. Martin Sarah K. Martin, MS, PhD, is a Director of Science and Regulatory Advocacy at PhRMA and leads the organization’s Real-World Evidence, Cell and Gene Therapies, and Human Drug Review Program regulatory advocacy efforts. Before joining PhRMA, Sarah served as the Director of Regulatory Science and Policy for the American Association for Cancer Research and as a Science Policy Fellow for the American Society for Biochemistry and Molecular Biology. Sarah was born and educated in Lexington, Kentucky, where she earned degrees in Animal Science (BS), Animal Nutrition (MS), and Molecular and Cellular Biochemistry (PhD) from the University of Kentucky. Sarah has always been a great lover of animals and currently has three dogs, a horse, and a saltwater fish tank at home taking up much of her free time.

Recent Posts

What you should know about real-world evidence and drug development

By Sarah K. Martin  |    December 19, 2022
Recently, industry leaders, regulators, academics, data partners, and patient advocates gathered in Washington, D.C., to discuss using real-world data and real-world evidence for regulatory...   Read More

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