If you are pregnant or nursing, talk with your health care professional about whether to enroll in pregnancy safety or ...

With this step, DGFT is enhancing ease of doing business for pharmaceutical exporters while ensuring regulatory coherence. Accordingly, the provisions under Para 2.76 of the Handbook of Procedures ...

The FDA removed previously issued draft guidance on diversity in clinical trials from its website without public notice or ...

Tazbaz was director of the FDA’s Digital Health Center of Excellence for two years, leading key policies on artificial ...

While sleep supplements can be beneficial, the lack of regulation means consumers are not assured of a safe and effective product.

AbbVie (ABBV), a large drug maker, is jumping 8% after the company provided significantly higher-than-expected 2025 earnings ...

What will the industry face or achieve in 2025? These trends will be critical in medical device cybersecurity.

As part of the education program, Huddleston and other AFIA officials reviewed the status of Environmental Protection Agency ...

The Commerce Ministry has withdrawn the track and trace provisions for pharmaceutical exports, aligning with the Ministry of Health’s regulations under Drug Rules 1945. The system, initiated in 2011, ...

In 2022, Congress passed the FDAMA 2.0, which Kennedy helped introduce and Pres. Joe Biden signed into law. The law removes a requirement under the Federal Food, Drug and Cosmetic Act for mandatory ...

Susan Krause of Rosemount alleges New Jersey-based Integra LifeSciences pressured her to lie to regulators. Integra says ...

When politicians subordinate scientific institutions to electoral interests, they undermine immediate public health efforts ...