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BioWorld - Wednesday, December 24, 2025
Home » Topics » Regulatory » Policy

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FDA icons and doctor

New FDA fast track for repurposed drugs?

Sep. 23, 2025
By Mari Serebrov
No Comments
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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COVID-19 vial, syringe and vaccine card

Decide on COVID-19 shot at your own peril: ACIP

Sep. 22, 2025
By Randy Osborne
No Comments
The second day’s meeting of the U.S. CDC’s Advisory Committee for Immunization Practices (ACIP) took up guidelines related to COVID-19 vaccines, of which an outspoken skeptic is Health and Human Services Secretary Robert Kennedy – who in June fired all 17 members of ACIP and replaced them with names more to his liking.
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COVID-19 vial, syringe and vaccine card

Decide on COVID-19 shot at your own peril: ACIP

Sep. 19, 2025
By Randy Osborne
No Comments
The second day’s meeting of the U.S. CDC’s Advisory Committee for Immunization Practices (ACIP) took up guidelines related to COVID-19 vaccines, of which an outspoken skeptic is Health and Human Services Secretary Robert Kennedy – who in June fired all 17 members of ACIP and replaced them with names more to his liking.
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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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Monarez gives her side of how she was fired from the CDC

Sep. 17, 2025
By Mari Serebrov
No Comments
For enquiring minds that want to know, Susan Monarez laid out the details Sept. 17 of how she was fired as CDC director for the Senate Health, Education, Labor and Pensions Committee.
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Susan Monarez speaks at Senate HELP hearing

ACIP meeting cause for consternation at US Senate hearing

Sep. 17, 2025
By Mari Serebrov
No Comments
The Sept. 17 U.S. Senate Health, Education, Labor and Pensions Committee hearing on the CDC is throwing even more shade on the upcoming meeting of the agency’s reconstituted Advisory Committee for Immunization Practices (ACIP), which is expected to recommend changes to the childhood vaccine schedule.
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China in red on globe
Bio Hong Kong 2025

US chaos positions China as more dependable leader

Sep. 16, 2025
By Tamra Sami
No Comments
China was already making strides to lead the biotechnology industry in many key areas such as cell therapies and AI, but the chaotic nature of the Trump administration and the turmoil in the U.S. has catapulted China’s status as a more “dependable” partner, presenters said during the Bio Hong Kong conference, Sept. 10 to 13.
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Kim Kyung-ah, CEO, Samsung Bioepis

South Korea to hike biosimilar approval fees, slash review times

Sep. 16, 2025
By Marian (YoonJee) Chu
No Comments
South Korea’s Ministry of Food and Drug Safety announced Sept. 12 plans to significantly raise drug application fees for biosimilars but slash their review times starting next year.
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Halt of biopharma investment prompts emergency UK hearing

Sep. 16, 2025
By Nuala Moran
No Comments
The U.K.’s failure to join the dots from discovery research to patient access to innovative drugs was cited repeatedly by pharma leaders, who were called to an emergency hearing in parliament on Tuesday to explain decisions to pull out of promised capital investments.
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