On March 20, 2024, The USPTO issued an alert, notifying practitioners that the USPTO had developed training materials for patent examiners regarding searching for prior art in FDA and NIH databases.[1 ...
Two advisory panels from the Food and Drug Administration will meet Tuesday and Wednesday to discuss the agency’s strategy to reduce adverse outcomes of opioid use, including review of its current ...
(The Hill) — An internal Food and Drug Administration (FDA) report examining what went wrong with the federal government’s response to the infant formula shortage earlier this year found 15 different ...
This Auditing for GMP course is specifically designed to address the challenges of GMP auditing for the pharmaceutical industry and present the basic competencies required to effe ...
Dublin, Jan. 07, 2026 (GLOBE NEWSWIRE) -- The "CSA in Practice: How to Build Defensible Evidence the FDA Actually Wants to See (Jan 13, 2026)" training has been added to ResearchAndMarkets.com's ...
The U.S. Food and Drug Administration announced this week that it deployed a generative AI tool called Evidence-based Learning System Assistant. After a low-profile pilot that delivered measurable ...
CHARLOTTESVILLE, Va.--(BUSINESS WIRE)--LumaCyte, a trailblazer in advanced label-free cellular bioanalytical technology and instrumentation, proudly announces the launch of the Laser Force Cytology™ ...
SEATTLE, Jan. 2, 2026 /PRNewswire/ -- BrainSpace, a medical technology company building automated solutions for neuro injury, illness and degeneration, today announced that the U.S. Food and Drug ...
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