The US Department of Health and Human Services on Wednesday announced a program and funding opportunity through the Advanced Research Projects Agency for Health (ARPA-H) called the ...
The US Food and Drug Administration (FDA) has issued notices inviting subject-matter experts and consumer representatives to volunteer for its advisory committees. The move comes after the role of FDA ...
Welcome to Regulatory Reconnaissance, your regulatory news and intelligence briefing.
A panel of regulators convened at the 2026 RAPS Convergence to discuss several initiatives underway in Europe to help ...
CHARLOTTE, NC — Whether the US Food and Drug Administration (FDA) will accept clinical evidence from outside the United States (OUS) depends on if the investigations followed good clinical practice ...
Food & Nutrition US packaged food makers could help cut diet-related deaths, study shows (Reuters) Potential infant formula illnesses probed in the UK (Food Safety News) FDA identifies listeria, E.
Euro Roundup: EMA officials argue against making single pivotal trials the ‘rigid, default position’
Emer Cooke and other EMA leaders have weighed into the debate about whether sponsors should run one or two pivotal trials, arguing that the decision should be informed by the evidence needed to show a ...
This webinar will walk you through how to apply the FDA's CSA's risk-based principles to AI, and what that looks like in practice, using a validated requirement conflict detection AI agent as a ...
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