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BioWorld - Monday, April 13, 2026
Home » Authors » Mari Serebrov

Articles by Mari Serebrov

Vaccine vial and syringe

Latest ACIP recommendations added to CDC vaccine schedules

Oct. 6, 2025
By Mari Serebrov
No Comments
Even though the U.S. CDC is operating on a skeleton crew due to the partial government shutdown, it is updating its immunization schedules to adopt the COVID-19 and chickenpox vaccine recommendations the Advisory Committee on Immunization Practices (ACIP) made at its September meeting.
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Global vaccine illustration

So far, ACIP vaccine recommendations in line with the world

Oct. 2, 2025
By Mari Serebrov
No Comments
While the discussions and votes at the past two meetings of the U.S. CDC Advisory Committee for Immunization Practices (ACIP) have generated a lot of controversy and resulted in some states and medical groups issuing their own vaccine schedules, the truth is that the newly reconstituted committee’s recommendations to date are still in line with, or more generous in some instances than, global norms.
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Laptop displaying FDA logo

New FDA submissions stalled during US government funding lapse

Oct. 1, 2025
By Mari Serebrov
No Comments
Caught between the start of fiscal 2026 and a congressional funding standoff that shut down much of the U.S. federal government Oct. 1, the FDA will not be able to collect 2026 user fees until Congress agrees on a continuing resolution or a 2026 appropriations bill.
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US Capitol at night

HHS rolls the numbers as shutdown looms for US government

Sep. 30, 2025
By Mari Serebrov
No Comments
Despite down-to-the-wire negotiations, the odds are that parts of the U.S. government will shut down at midnight Sept. 30, as Senate Democrats refused to support a seven-week, clean continuing resolution already passed by the House to keep the government funded while Congress hammers out fiscal 2026 spending bills.
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DNA in drug capsules

FDA continues to build regenerative medicine pathway

Sep. 26, 2025
By Mari Serebrov
No Comments
The U.S. FDA released a trio of draft guidances to help sponsors in developing and monitoring cell and gene therapies, as well as other regenerative medicine therapies.
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Prescription bottle with dollar sign shadow

MFN pricing model under White House review

Sep. 26, 2025
By Mari Serebrov
No Comments
As President Donald Trump promised again in a Sept. 23 media briefing, most-favored-nation (MFN) prescription drug pricing could soon come to America.
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Hand holding a pink slip or termination notice against a blurred office background

More US federal layoffs, future of SBIR on the table

Sep. 25, 2025
By Mari Serebrov
No Comments
The struggle to avoid a partial U.S. government shutdown at midnight Sept. 30 is getting a lot of attention, as the stakes increase every day of the political standoff. Meanwhile, Sept. 30 also could be the end of the 43-year-old Small Business Innovation Research (SBIR) program, which has been a funding boon for biotech and med-tech startups, if Congress can’t come together on a reauthorization bill.
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FDA icons and doctor

New FDA fast track for repurposed drugs?

Sep. 23, 2025
By Mari Serebrov
One Comment
Breaking with its long-held, oft-recited mantra that observational studies are great for generating hypotheses but not as evidence for approval, the U.S. FDA is initiating the approval of leucovorin calcium tablets for patients with cerebral folate deficiency, a neurological condition that affects folate transfer into the brain.
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ACIP delays vote on hep B vaccine, proposal not as bad as feared

Sep. 18, 2025
By Mari Serebrov
No Comments
Despite some expectations that the U.S. CDC’s Advisory Committee for Immunization Practices (ACIP) would dramatically change the childhood vaccine schedule for hepatitis B, the committee is poised to vote Sept. 19 on a much smaller change that would move the current birth dose to 1 month for infants born to mothers who test negative for hepatitis B.
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Pediatric exam

Pediatrics group absent from US CDC vaccine discussion

Sep. 18, 2025
By Mari Serebrov
No Comments

The American Academy of Pediatrics (AAP) and a few other medical professional groups were no-shows at the Sept. 18 meeting of the U.S. CDC’s Advisory Committee for Immunization Practices. The absence of the liaison groups was noted, especially that of the AAP. In opening the two-day meeting, ACIP Chair Martin Kulldorff said he lamented that the AAP has ended its association with the committee.


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