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Conagra to sell seafood brands Van de Kamp’s and Mrs Paul’s for $55M (Food Dive)
How Nerds Gummy Clusters became a big hit in candy (Food Dive)
California Bill Would Remove Ultra-Processed Foods from School Lunches (Food Safety)
Government, Regulatory & Legal
RFK Jr.’s chronic disease agency would eliminate or reduce funding for some prevention programs (STAT)
Philanthropies rush to save measles surveillance network pushed to brink of collapse by U.S. cuts (STAT)
FDA reassures rare disease advocates that ‘being flexible’ is plan for gene therapy (STAT)
Pharma imports into the US return to normal after March tariff stockpiling (Endpoints)
Judge rules J&J unit must pay $442M in antitrust case (MedTech Dive)
Regulatory Recon is our regular intelligence briefing for the regulatory affairs space, bringing you the top regulatory, biopharma and medtech news stories from around the globe. Regulatory Recon is published each week on Monday, Tuesday and Thursday.
A story’s inclusion in Regulatory Recon does not imply endorsement by Regulatory Focus or RAPS.
Three major pharmaceutical industry groups—two in the US and one in India—have called for changes to the US Food and Drug Administration's (FDA) Scale-Up and Post-Approval Changes (SUPAC) guidelines. They believe these guidelines should be updated to reflect more modern manufacturing methods and better align with International Council for Harmonisation (ICH) standards.
Patients with breast cancer said faster approval times for oncology products, as a trade-off for evidentiary certainty, is most permissible in situations where there are no treatment alternatives, the results from a recent qualitative study suggest.