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BioWorld - Thursday, February 26, 2026
Home » Authors » Mari Serebrov

Articles by Mari Serebrov

ACIP expands again, but no new infectious disease experts added

Jan. 13, 2026
By Mari Serebrov
No Comments
U.S. Health and Human Services Secretary Robert Kennedy has once again expanded the CDC’s Advisory Committee on Immunization Practices (ACIP), this time adding two more ob-gyns to the membership list. As a result, the ACIP, which can have up to 19 members, now numbers 13, three of whom are ob-gyns.
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Pen and paper

Pace of EOs slows, but still wields big impact

Jan. 13, 2026
By Mari Serebrov
No Comments
Perhaps the biggest indicator of U.S. President Donald Trump’s activism in his second term is the 225 executive orders (EOs) he issued in 2025. The pace of those orders seems to have slowed, with “only” 16 released in the last quarter of the year. Four of the recent EOs could impact drug and device companies in a myriad of ways.
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FDA takes flexibility, modernization steps in CGT, Rx development

Jan. 12, 2026
By Mari Serebrov and Nuala Moran
No Comments
Moving away from a one-size-fits-all approach, the U.S. FDA's CBER released details Jan. 11 about how it’s leveraging its growing experience with cell and gene therapies (CGTs) to exercise greater regulatory flexibility in chemical, manufacturing and control requirements for the products.
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Yellow umbrella in a storm

High pressure areas predicted for 2026 medical device landscape

Jan. 8, 2026
By Mari Serebrov
It doesn’t take a meteorologist to see the storm clouds of uncertainty that will continue to roll in on health care across the globe this year. While the prospects for the medical device industry may be sunnier than for other aspects of health care, some high pressure areas likely will present challenges.
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Policy

Appeals court says no to cap on indirect costs in NIH grants

Jan. 8, 2026
By Mari Serebrov
No Comments
Unless the U.S. Supreme Court steps in to reverse the decision, the NIH’s attempt to cap indirect costs at 15% in all its grants is dead. The U.S. Court of Appeals for the First Circuit upheld a permanent injunction Jan. 5 that was issued by a lower court, vacating an NIH supplemental guidance imposing the across-the-board cap both retroactively and prospectively.
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U.S. vaccine illustration

Industry considering options amid US vaccine upheaval

Jan. 7, 2026
By Mari Serebrov
No Comments
The chaos Health and Human Services Secretary Robert Kennedy has injected into the U.S. vaccine market could have long-term consequences as vaccine makers reevaluate business decisions and pipelines.
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Appeals court says no to cap on indirect costs in NIH grants

Jan. 6, 2026
By Mari Serebrov
No Comments
Unless the U.S. Supreme Court steps in to reverse the decision, the NIH’s attempt to cap indirect costs at 15% in all its grants is dead. The U.S. Court of Appeals for the First Circuit upheld a permanent injunction Jan. 5 that was issued by a lower court, vacating an NIH supplemental guidance imposing the across-the-board cap both retroactively and prospectively.
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Yellow umbrella in a storm

Stormy year in biopharma forecast

Jan. 6, 2026
By Mari Serebrov
No Comments
It doesn’t take a meteorologist to predict another stormy year for the biopharma sector, not just in the U.S., but also in Europe. Lurking within those storms, though, could be a few silver linings.
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US vaccine schedule slashed to international standards

Jan. 5, 2026
By Mari Serebrov
No Comments
With the stroke of a pen and no input from the CDC’s Advisory Committee for Immunization Practices, acting CDC Director Jim O’Neill cut the number of vaccines the agency routinely recommends for children to 11 on Jan. 5, down from 17 in 2024.
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2025 US regulatory word cloud
The year in review

Year marked by chaotic regulatory uncertainty in US

Dec. 31, 2025
By Mari Serebrov
No Comments
If the 2025 U.S. life sciences regulatory scene were to be summed up in one word, it would have to be uncertainty. Two words might be more definitive – chaotic uncertainty.
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