The FDA released a draft guidance document that provides a regulatory framework for sponsors to utilize minimal residual ...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 ...
Central retinal artery occlusion can result in permanent vision loss. Effective treatment is lacking. We conducted a phase 3, double-blind, double-dummy, randomized, controlled trial involving ...
In today's healthcare environment, securing regulatory approval is only the beginning. The real challenge lies in ensuring ...
Verifying an extensible processor is more than a one-step process, especially when software compatibility is important.
MoonLake requested a Type B meeting with the U.S. Food and Drug Administration (FDA) to obtain regulatory clarity and discuss the clinical evidence strategy for submission of a Biologic License ...
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.
In the draft guidance, the agency discusses how sponsors can leverage MRD and complete response rates as near-term efficacy measures and speed new therapies to market.
You answer the call of the wild. You’re happiest with your hands in the dirt, and you often prefer plants to people (but we won’t tell). You spend winters organizing your potting shed, thumbing ...
As Hytale develops further in Early Access, developer Hypixel Studios has opened up about the future of world generation with ...
Africa stands at the edge of a historic demographic shift. By 2050, one in three young people in the world will be African. This represents an extraordinary opportunity for the continent to shape ...
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