The U.S. Food and Drug Administration is replacing animal testing with human-relevant methods, including artificial intelligence, when developing monoclonal antibody therapies and other drugs.

“In this capacity, he will serve as a trusted advisor to the FDA Commissioner and other senior officials on cross-cutting and emerging medical and scientific issues impacting regulatory science ...

A new international study suggests that ancient viral DNA embedded in our genome, which were long dismissed as genetic "junk, ...

FDA and NIH will hold a joint nutrition regulatory science workshop on December 17-18, 2024. The goal of the workshop is to highlight how nutrition and science can generate evidence and data to ...

Regulatory science is an emerging field focused on developing the scientific tools, standards, and approaches needed to assess the safety, efficacy, quality, and performance of products regulated ...

A report is challenging decades of scientific findings to undermine the EPA’s authority.

This session, scheduled for Tuesday, November 5, will bring together industry, academia and regulatory bodies to drive advancements in regulatory science and accelerate digital pathology adoption ...

When Lawrence Carter started his Master of Science in Biotechnology Innovation and Regulatory Science (BIRS) with Purdue, he was in the middle of several big life changes. For one, he was thinking ...

FDA will contribute regulatory science expertise to the program, while NIH will provide infrastructure for scientific research, with experts in chronic disease, nutrition, toxicology, risk ...

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