Discover how quality-driven drug development and AI accelerate safer medicines, reduce risk, and improve patient outcomes.

The Food and Drug Administration is a government agency that regulates certain food, drugs, cosmetics, and medical products.

For the first time, FDA regulators will be able to see what’s happening in a clinical trial, looking at endpoints in the ...

Johnson & Johnson is using artificial intelligence to slash by half the time it ‌takes to generate new leads for developing ...

Barbara Slusher explains the hit-to-lead optimization process, high-throughput screening, and the role of AI and organoids in ...

Researchers at Kent have established a computational protocol that could accelerate the development of more effective ...

Researchers investigating a widely used medication have uncovered an unexpected cellular process that may interfere with ...

Explaining Drugs To The Youngest Sibling. Hey there! I'm Hew Moran, a content creator who combines my passion for gaming, YouTube, and comedy into skits you’ll find hilariously relatable. On my ...

Nobel laureate Sir Michael Houghton and colleagues at Applied Pharmaceutical Innovation (API) outline how rigorous early testing, smart IP and regulatory planning, and scalable CMC choices can help ...

Early-stage drug development worldwide has nearly doubled over the past decade and shifted from a U.S.-dominated model to a dual hub centered in the United States and China, according to new research ...

Lizzy Lawrence leads STAT’s coverage of the Food and Drug Administration. She was previously a medical devices reporter. You can reach Lizzy on Signal at lizzylaw.53. WASHINGTON — The Department of ...