The majority are in the very early preclinical stage of development, but applications for regulatory approval have been ...

The FDA’s framework for AI regulation, while robust for premarket evaluation, would benefit from more specific mechanisms for continuous monitoring of AI performance in diverse real-world settings.

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

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

The move aims to eliminate duplication, reduce compliance burdens on exporters, and ensure consistency with global serialization standards.

The Commerce Ministry has withdrawn the track and trace provisions for pharmaceutical exports, aligning with the Ministry of Health’s regulations under Drug Rules 1945.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

Indonesia is ramping up efforts to reduce its reliance on imported pharmaceutical raw materials and strengthen its local drug industry. The government is rolling out policies to encourage domestic ...

Merck on Friday said the recommendation from the European Medicines Agency's Committee for Medicinal Products for Human Use covers the 21-valent conjugate vaccine for immunization for the prevention ...

Meloxicam is a nonsteroidal, anti-inflammatory molecule developed with Axsome’s Molecular Solubility Enhanced Inclusion ...

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

KORU Medical Systems (NASDAQ: KRMD) (“KORU Medical” or the “Company”), a leading medical technology company focused on the ...

The FDA’s nod for suzetrigine bolsters confidence in the pharmaceutical industry’s strategy to target sodium channels.