FDA again bypasses advisers to remove black-box warnings from menopause treatments Some experts express concern about ‘lack of transparency’ as agency removes warnings on three estrogen patches The Guardian - US · Oct 30
As RFK’s lifestyle seeps into policy, some fret over long-term effect When Health and Human Services Secretary Robert F. Kennedy Jr. took the helm of the department in February 2025, he pledged to remove special interests from HHS and chart a new path focused on “gold-standard science.” He made his core policy interests clear in November 2024, even before he was President… Roll Call · May 15
Top-down approach has Congress AWOL on FDA, experts say - Roll Call Since President Donald Trump took office, the FDA has lost about 20 percent of its staff through reduction-in-force efforts. Roll Call · Jan 8
Judge temporarily blocks agencies from removing health data - Roll Call Doctors for America sued after the removal of several webpages, including guidance related to STIs and HIV. Roll Call · Feb 11, 2025
RFK Jr will cut prescription drugs and increase weed and psychedelics access Trump’s health department pick has expressed distrust of pharmaceuticals and attacked ‘suppression of psychedelics’ The Guardian - US · Nov 25, 2024
Chevron doctrine ruling a ‘gut-punch’ for US health and environment – experts Decision that overturned convention of deference to federal agencies could upend regulations on tobacco, drugs and medical bills The Guardian - US · Jul 6, 2024
Gene therapy for muscular dystrophy stirs hopes and controversy The FDA is considering greenlighting the experimental treatment under its accelerated approvals program. Some critics point out the therapy isn't yet proven to work and may be costly. WEKU · May 2, 2023
FDA has new leverage over companies looking for a quicker drug approval The Food and Drug Administration has new tools to hold drug companies accountable for promises they make about medications. But the agency has yet to show its hand in using this new power. WEKU · Mar 3, 2023
Speedier drug approvals hit slowdown as FDA faces scrutiny The Food and Drug Administration is slowing its use of a pathway that expedites the approval of promising drugs The Independent UK · Dec 7, 2022
Read Why Pfizer Is Limiting Supply Of Paxlovid For Combination Studies: Bloomberg Amid rising concerns over the potential development of resistance to Pfizer Inc's (NYSE:PFE) COVID-19 pill Paxlovid, the company has declined to supply researchers with the antiviral for use in combination studies, according to a Bloomberg report. Researchers say that Paxlovid combined with other drugs might stave off resistance. Pfizer hasn't started any combination… Benzinga · May 19, 2022