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Understanding Messenger RNA Vaccines in Humans & Animals
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Human Health, Biodefense and Vaccines  •  Toolkit  •  March 16, 2025
Every cell in the human body contains mRNA, which directs your body to make proteins. mRNA immunizations teach your body how to make its own medicine for a virus or other pathogen.
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BIO Files Amicus Brief Challenging CMS’s IRA-Implementing Guidance
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Amicus Brief  •  March 14, 2025
BIO filed an amicus brief in the U.S. District Court for the District of Columbia, supporting plaintiff Teva Pharmaceuticals' position that the definition of Qualifying Single Source Drug (QSSD) in CMS's IRA-implementing Guidance violates the statutory definition, resulting in significant harm to biopharma innovation. By way of the Inflation Reduction Act (IRA), Congress directed the Centers for Medicare & Medicaid Services (CMS) to "negotiate" with manufacturers the maximum prices of drugs that CMS had previously identified as top-spend medications already marketed for a certain number of years. However, genuine negotiation does not take place under CMS's Drug Price Negotiation Program (DPNP). CMS sets the selected medication's maximum price and by a certain deadline, the manufacturer must either agree or face paying a penalty "excise tax" until there is agreement on the price. The brief argues that CMS has gone beyond its authority via its Guidance, veering from the plain text of the IRA and redefining the definition of a "Qualifying Single Source Drug" or QSSD. Their redefinition of QSSD allows for drug products that would have been ineligible for negotiations to be swept into the DPNP. Rather than promoting innovation, the CMS guidance deters it, disincentivizing the development of new drug products, particularly orphan drugs with new indications.
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BIOPAC: BIO Board Member Enrollment Form
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Plea to Congress on PPRV; women's health
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Good Day BIO Newsletter  •  March 10, 2025
BIO President & CEO John F. Crowley writes Congress to urge PPRV passage; plus a deep dive into the impact of autoimmune disease on women. (761 words, 3 minutes, 48 seconds)
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BIO Letter to Congressional Leadership on the Give Kids a Chance Act & Reauthorization of the Pediatric Priority Review Voucher Program (PPRV)
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Letters, Testimony & Comments  •  March 7, 2025
One thing that we can all agree on is the need to give our children a fighting chance so they can lead long and productive lives. That is why it is critical to pass the bipartisan Give Kids a Chance Act and ensure the Pediatric Priority Review Voucher Program (PPRV) is reauthorized. This program will provide greater certainty to small biotech companies, but more importantly, hope to children and families living with rare diseases.
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John F. Crowley's One-Year Anniversary Letter to BIO Membership.
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Letters, Testimony & Comments  •  March 4, 2025
Dear Colleagues, This month marks my one-year anniversary as BIO's CEO. Like most of us in biotech, this post has been a labor of love. At no time in my 25-year career in this industry have I ever witnessed such awe-inspiring science. Today, we increasingly have the tools, talents, and technologies to address a range of challenges in human health, the environment, and food security – allowing us to alleviate an enormous amount of human suffering. These stunning advancements, though, are at a crossroads. Not only does the U.S. face intense global competition as the world's center of excellence in biotechnology innovation, but we also face a series of societal and political challenges that threaten key elements of our industry's foundation. In short, we are at an inflection point. We can either continue with a system that unnecessarily slows progress and distorts our choices, or reform it to better benefit patients and those in need.Eight years ago, President Trump highlighted the shortcomings of our drug approval system in his first address to a joint session of Congress. I recall it vividly, because I was there. As you may know, my daughter Megan has Pompe disease, a rare neuromuscular disorder. During his remarks, the President highlighted Megan’s condition and spoke directly to her in the audience. He added, “the slow and burdensome approval process at the Food and Drug Administration keeps too many advances, like the one that saved Megan’s life, from reaching those in need.” He was right then, just as he is right today. Yet the way that government reforms the FDA – as well as other regulatory bodies that oversee our industry – must strengthen these agencies, not weaken them. We have an opportunity now to accomplish just that, and we must seize it. "No organization is better positioned or more intensely focused on creating (and restoring) a strong and expedient innovation ecosystem than BIO." The Best Job You Could Ever HaveAs someone who…
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A 'pill penalty' fix and bipartisan calls for PBM reform
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Good Day BIO Newsletter  •  March 3, 2025
A busy week in Washington, D.C., brought legislation to fix the Inflation Reduction Act “pill penalty,” bipartisan calls for PBM reform, and BIO CEO John F. Crowley explaining why Congress needs to act to support rare disease drug development. (1012 words, 5 minutes, 3 seconds)
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BIO Comments on Office of Management and Budget (OMB) Statistical Policy Directive No. 8 North American Industry Classification System (NAICS)-Request for Comments on Possible Revisions for 2027 (USBC–2024–0032)
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Letters, Testimony & Comments  •  February 28, 2025
Re: BIO Comments on Office of Management and Budget (OMB) Statistical Policy Directive No. 8 North American Industry Classification System (NAICS)-Request for Comments on Possible Revisions for 2027 (USBC–2024–0032)Dear Ms. Orvis,The Biotechnology Innovation Organization (BIO) welcomes this opportunity to respond to the request for public comment from the Office of Management and Budget (OMB), on behalf of the Economic Classification Policy Committee (ECPC), as a part of the review of the 2022 North American Industry Classification System (NAICS) for potential revisions to be made to the structure and content of the NAICS for 2027.
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2025 BIO International Convention Preview & ​Exhibitor Basics
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Webinars  •  February 27, 2025
Join Sydney Williams, BIO Senior Manager, Exhibit Sales & Systems, for a webinar to walk exhibitors through the tools needed to plan for the 2025 BIO International Convention. This webinar gives our exhibitors the resources to have an impactful presence in Boston. The following topics are discussed: Exhibitor resource centerExhibitor tools and resourcesTips to maximize your event experience in Boston
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2025 Exhibit Sales Booth

BIO Applauds Introduction of Bipartisan Bill to Eliminate the Pill Penalty
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Press Release  •  February 25, 2025
Legislation will help spur the development of lifesaving treatments and cures WASHINGTON D.C. (February 25, 2025) – John Crowley, president and CEO of the Biotechnology Innovation Organization (BIO), released the following statement after Representatives Gregory Murphy (R-NC), Don Davis (D-NC) and Richard Hudson (R-NC) introduced the “Ensuring Pathways to Innovative Cures (EPIC) Act,” bipartisan legislation that would eliminate the pill penalty in the 2022 Inflation Reduction Act:“For decades small molecule medicines for that come in a pill or tablet have been recognized for improving patient adherence, being easier to take, and more broadly accessible to those who need them. As a result, hundreds of such therapies have been developed for the treatment of devastating diseases ranging from cancer to mental illness.  Today, instead of building on years of biomedical progress, some innovator companies and investors are now being forced to pull away. The Inflation Reduction Act targets small molecules for government price setting years earlier than other medicines, sending the wrong message to everyone trying to develop new breakthrough treatments in a pill or tablet formulation. Instead of arbitrary and unnecessary market distortions guiding drug development decisions – we should be following the science and prioritizing getting important new medicines to patients.“On behalf of America’s patients and biotech innovators. I’d like to thank Representatives Gregory Murphy (R-NC), Don Davis (D-NC) and Richard Hudson (R-NC) for their leadership on this important issue. This bipartisan legislation will eliminate the pill penalty and help ensure science and researchers – not government bureaucrats – determine the possible treatments innovator companies pursue. I hope Congress will act quickly on this legislation and protect the development of future treatments and cures that patients are counting…
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