COMMUNITY NEWS CBO Analysis Shows Significant Impact of NIH Funding Cuts and FDA Delays on Drug Development

What It Means for Georgia

A new report released July 18, 2025, by the Congressional Budget Office (CBO) provides the first quantitative look at how changes to federal research funding and regulatory timelines could impact pharmaceutical innovation in the U.S.


Key Findings

The report models two policy scenarios: a permanent 10% cut to NIH's external preclinical research funding and a nine-month extension of FDA review timelines for new drug applications.


NIH Funding Cuts

A 10% permanent cut to NIH-funded preclinical research would lead to:

  • ~2 fewer new drugs entering the market each year
  • 1 fewer drug in the first decade
  • 9 fewer drugs in the second decade
  • 20 fewer drugs per decade by the third decade and beyond


FDA Review Delays

  • A 9-month increase in FDA review times would result in:
  • 3 fewer drugs in the first decade
  • 10 fewer drugs per decade in the second and third decades
  • A 2% overall annual reduction in drug approvals


Implications for Georgia’s Life Sciences Ecosystem


Research Impact:
Georgia institutions such as Emory University, Georgia Tech, Augusta University, and Morehouse School of Medicine rely on NIH funding to drive foundational biomedical research. A permanent NIH funding cut could weaken the early-stage research pipeline and limit opportunities for academic-commercial partnerships.


Biotech Vulnerability:
Extended FDA review times pose a serious challenge for Georgia’s small and emerging biotech companies—particularly those operating in Augusta, Atlanta, and Athens—with limited capital to absorb regulatory delays. This may force earlier exits, reduce investor confidence, or deter innovation altogether.


Economic Risk:
Georgia’s position as a growing life sciences hub could be jeopardized. States with stronger public-private investment ecosystems may be better positioned to weather these changes—intensifying regional competition for jobs, talent, and investment.


Industry Perspective

"Without the foundational support of NIH-funded research, Georgia’s innovation engine would stall. Our universities, startups, and investors all rely on a robust federal research ecosystem to drive discoveries from bench to bedside," said Maria Thacker Goethe, President & CEO of Georgia Life Sciences. "This report confirms what many of us already feared—policy decisions made in Washington have ripple effects that directly impact patients, jobs, and innovation here in Georgia."


Looking Ahead

The CBO report makes it clear: NIH funding and FDA efficiency are not abstract policy issues—they shape the future of health innovation in Georgia. As federal budget debates unfold, Georgia Life Sciences remains committed to advocating for sustained investments in research and a regulatory environment that supports timely, equitable access to new therapies.


Read the full CBO report: https://www.cbo.gov/publication/61373

December 10, 2025
Georgia Life Sciences has joined 43 state and regional life sciences organizations in signing a national Council of State Bioscience Associations (CSBA) letter calling on Congress to take immediate action on three bipartisan policy priorities that are essential to sustaining U.S. leadership in biomedical innovation and supporting patients nationwide. With Congress back in session and several critical programs at risk of expiring, the letter urges congressional leaders to advance the following provisions without delay: 1. Reauthorize the Rare Pediatric Disease Priority Review Voucher (PPRV) Program The PPRV program has been instrumental in incentivizing the development of therapies for children with rare and life-threatening conditions. Its lapse threatens to slow or halt research that families across the country are counting on. 2. Extend the SBIR/STTR Programs The Small Business Innovation Research (SBIR) and Small Business Technology Transfer (STTR) programs provide crucial early-stage capital for emerging biotech and medtech companies—many of them in Georgia. Without reauthorization, hundreds of innovative small businesses face uncertainty, jeopardizing new therapies, diagnostics, and technologies in the pipeline, 3. Advance PBM Transparency Reforms Greater transparency and accountability within pharmacy benefit manager (PBM) practices are needed to ensure that savings reach patients and employers. Reforming PBM operations is essential to strengthening access and affordability across the healthcare system. A Unified Message from the Life Sciences Community The sign-on letter reflects broad, bipartisan alignment across the national life sciences ecosystem: researchers, entrepreneurs, investors, patient advocates, and state associations all share a common message— these programs underpin America’s global competitiveness and are vital to patients who rely on continued scientific progress. Georgia Life Sciences has shared the letter with members of Georgia’s congressional delegation and will continue engaging with policymakers to emphasize the importance of swift action.
December 7, 2025
Georgia Life Sciences is proud to stand with patient advocates, providers, and employers across the state in urging Congress to take meaningful action on pharmacy benefit manager (PBM) reform. We recently signed on to a joint letter to Georgia’s Congressional Delegation stressing the urgent need for transparency, fair practices, and policies that ensure savings flow directly to patients.
December 4, 2025
Georgia Life Sciences’ CEO, Maria Thacker Goethe shares her perspective on the value of Georgia’s research universities in this month’s issue of Georgia Trend. “Georgia research institutions have felt a very significant impact from the federal rollbacks, specifically in NIH and NSF funding. Thacker Goethe’s message about the impact of research cuts is simple: Disruption shatters the foundational trust researchers have in grant continuity….” To read the full article, click here .
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