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BIO Office Hours: Grant Applications with PSC Biotech
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March 29, 2023
BIO Office Hours is a resource for BIO members to meet one-on-one with subject matter experts on business services. Are you applying for a government grant? Don't know where to start or how to best allocate your time and resources to complete the grant proposal and subsequent work? Not sure if your application satisfies all requirements? Schedule an office hour with a PSC Biotech Subject Matter Expert.   Schedule Office Hour
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BIO Statement to the U.S. International Trade Commission on COVID-19 Diagnostics and Therapeutics: Supply, Demand, and TRIPS Agreement Flexibilities
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Letters, Testimony & Comments  •  March 29, 2023

HHS on price controls, PBMs, and more
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Good Day BIO Newsletter  •  March 29, 2023
We recap what HHS Secretary Becerra said yesterday about everything from drug pricing to PBMs, and get ready for more hearings today, including the USITC’s hearing on the COVID IP waiver. (674 words, 3 minutes, 22 seconds)
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BIO Files Amicus Brief in U.S. ex rel. Scutte v. SuperValu Inc. at the Supreme Court of the United States
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Amicus Brief  •  March 28, 2023
BIO has filed an amicus brief in U.S. ex rel. Scutte v. SuperValu Inc., which addresses the issue of the intent requirement under the False Claims Act (FCA). Specifically, BIO urges the Court to uphold the view that a firm does not have the requisite intent to violate the FCA when its interpretation of a statute or regulation: (1) is “objectively reasonable,” and (2) no authoritative guidance cautions against it. A carefully calibrated FCA intent requirement is important to biotech companies, which operate in an environment of extreme regulatory complexity. Federal agencies frequently manage this complexity by pursuing a strategy of deliberate regulatory ambiguity (i.e., relying on non-binding guidance rather than statutory language or rulemaking). Ths approach has a number of advantages, but when coupled with a overly broad FCA intent requirement risks chilling beneficial conduct. In the absence of a sensible intent requirement, biotech companies will tend to adopt only the most conservative regulatory interpretations, resulting in innovation- and investment-stifling overdeterrence, with corresponding implications for access and patient health. BIO was joined in the brief by AdvaMed and the Medical Information Working Group.
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How Accelerated Approval works
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Good Day BIO Newsletter  •  March 28, 2023
In the lull before the hearing storm, listen to the new episode of the I am BIO Podcast, which explains why Accelerated Approval is so important for patients. Plus, we look at legislation that would increase tax breaks for R&D. (729 words, 3 minutes, 38 seconds)
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Accelerating Hope: The Pathway for Cures
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I am BIO Podcast  •  March 28, 2023
When people were dying from AIDS in the 1980s and 90s, Congress found a way to expedite the drug approval process and saved countless lives. Established in 1992, the Accelerated Approval Program allows the FDA to speed approval of drugs for patients with serious and life-threatening conditions. In this episode we talk with the father of children with a rare disease, a company CEO working to treat rare diseases and two policy experts on Accelerated Approval.
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Why we need new antifungals – fast
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Good Day BIO Newsletter  •  March 27, 2023
We’re gearing up for another busy week in Washington—but first, what USTR said about biotech corn on Friday and why we need to act on a rapidly spreading fungus. (450 words, 2 minutes, 15 seconds)
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340B Backgrounder
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Human Health, Government Price Setting  •  Toolkit  •  March 27, 2023
In 1992, with the support of the biopharmaceutical industry, Congress created the 340B Drug Pricing Program to help uninsured and vulnerable patients. As part of the law, drug manufacturers provide significant discounts on outpatient medicines and treatments to select eligible health care “covered entities” — often referred to as safety- net providers.
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What USTR and HHS said on Capitol Hill
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Good Day BIO Newsletter  •  March 24, 2023
Happy Friday. A busy week on Capitol Hill concludes with hearings covering key issues including Mexico’s biotech corn ban, expanding the COVID IP waiver, and upholding the purpose of Bayh-Dole—we have a quick recap. (641 words, 3 minutes, 12 seconds)
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‘Innovations like our vaccine can only happen in America’
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Good Day BIO Newsletter  •  March 23, 2023
A busy week continues with yesterday’s hearings on the price of Moderna’s COVID-19 vaccine, the proposed HHS budget, and important PBM transparency legislation—with lots of discussion on priority issues for BIO members. Highlights below—plus, what we would ask USTR today. (733 words, 3 minutes, 39 seconds)
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