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BioWorld - Tuesday, May 12, 2026
Home » Topics » Regulatory » Policy

Policy
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Guillain-Barré case puts Moderna norovirus vax trial on hold

Feb. 14, 2025
By Karen Carey
Amid an overall positive earnings report of $3.2 billion in 2024 revenues, Moderna Inc. disclosed that the U.S. FDA placed its norovirus vaccine on a phase III clinical hold due to a single adverse event of Guillain-Barré syndrome (GBS).
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Doctor with brain illustration, businessman with dollar sign illustration
Analysis

NIH funding plans threaten to derail ‘synergistic partnership’

Feb. 13, 2025
By Anette Breindl
A 15% cap on indirect cost reimbursement that was announced by the U.S. NIH has been stalled by a court order for the time being. But researchers remain deeply concerned about the attempt, and about the new administration’s adversarial approach to research and universities.
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Regulatory-US-FDA-HQ.png

Uncertainty builds amid Kennedy confirmation, Trump’s orders

Feb. 13, 2025
By Mari Serebrov
Coming as no surprise, the U.S. Senate’s Feb. 13 confirmation of Robert Kennedy as the next secretary of the Department of Health and Human Services (HHS) did nothing to ease the uncertainty hanging over the FDA and other HHS agencies.
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European Union flag with wooden gavel

EC drops AI liability directive for now

Feb. 12, 2025
By Mark McCarty
The European Commission’s proposal for an AI-specific liability law seemed destined to pile onto existing EU liability law, but the commission reported it will pull the legislative proposal dubbed the AI Liability Directive.
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Shipping container with flag of China

Speculations rise on US tariff impact on global pharma industry

Feb. 11, 2025
By Marian (YoonJee) Chu
For the pharmaceutical industry caught in the crosshairs of a potential trade war, the consequences of U.S. tariffs on China or Europe remain largely speculative, although both would be detrimental, according to a Korea Biotechnology Industry Organization (KoreaBIO) issue briefing Feb. 7.
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Globe showing Asia-Pacific region

Mixed reactions from Asia on biotech implications of Trump 2.0

Feb. 11, 2025
By Tamra Sami
“This current administration is like nothing that we've seen before,” said a managing partner of a global venture capital firm who spoke to BioWorld on the condition of anonymity. “President Trump’s first term was bad,” he said, “but nobody knows what’s coming.” “This is truly nationalism at its worst, because he won on the campaign [largely] to protect American jobs, claiming that Americans have been unfairly treated.” And it's not just China, he said, but India and other countries will also likely be affected.
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Indirect costs of NIH grants

Feb. 11, 2025
In fiscal 2023, the NIH spent more than $35 billion on nearly 50,000 competitive grants to more than 300,000 researchers at more than 2,500 universities, medical schools and other research institutions across the nation. Of this funding, the NIH said about $26 billion was spent on direct research costs, while $9 billion was allocated to help cover “facilities and administration” through the agency’s indirect cost rate.
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Woman holding display of business, regulatory icons

BIO CEO 2025: Navigating from policy to innovation to patients

Feb. 11, 2025
By Karen Carey
The fast pace in which the Trump administration has rolled out changes to how government and businesses operate – a disruptive effort that appears to be creating a new world order – has caught the attention of biopharma industry leaders who spoke Tuesday at the Biotechnology Innovation Organization’s CEO and Investor Conference in New York.
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Dollar sign dropper and test tube

Court orders full stop to US NIH slashing of indirect rates

Feb. 11, 2025
By Mari Serebrov
The immediate implementation of the U.S. NIH’s guidance to cut indirect costs included in its grants to 15% was quickly halted late Feb. 10 when a federal district judge granted a nationwide temporary restraining order in two separate challenges to the cuts that were to go into effect that day on all existing and new NIH grants.
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Artificial intelligence and digital health icons

European Commission provides guidance for AI Act

Feb. 11, 2025
By Mark McCarty
The European Commission issued a set of guidelines for the use of AI as a supplement to the EU’s Artificial Intelligence Act, a document of which chatbot developers will want to take note.
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