The FDA released a draft guidance document that provides a regulatory framework for sponsors to utilize minimal residual ...
The Institute for the Advancement of Food & Nutrition Science publishes a list of general principles it hopes will inform any ...
In today's healthcare environment, securing regulatory approval is only the beginning. The real challenge lies in ensuring ...
9don MSN
The best Persona games, ranked
With Persona 3 Reload and Persona 5 Royal released, we rank the 12 best Persona games to see how the classics stack up ...
MoonLake requested a Type B meeting with the U.S. Food and Drug Administration (FDA) to obtain regulatory clarity and discuss the clinical ...
As 2026 dawns, look for HHS Secretary Robert F. Kennedy Jr. to ramp up his assault on vaccines using policy-based evidence making and altering Vaccine Court standards.
The head of the Department of Health and Human Services has spent decades promoting vaccine skepticism and has now revamped the US childhood immunization schedule to have one-third fewer recommended ...
In the draft guidance, the agency discusses how sponsors can leverage MRD and complete response rates as near-term efficacy measures and speed new therapies to market.
Recent research published in the journal Political Behavior shows that Americans largely prioritize the severity of a violent act over the perpetrator’s political identity when determining punishment.
CES 2025 is now well underway and we're live at the show –here's all of the latest tech news.
Coupling biomarker-guided screening with a targeted treatment bundle reduced newborn mortality, hospital stays, and other complications over standard care, according to a recent study.
12don MSN
Insurance data can help fill gaps between longer medical trials for patients up against the clock
Randomized clinical trials remain the gold standard for establishing a medication's effects, producing the evidence by which ...
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