A top official at the Food and Drug Administration recently overruled government scientists on the availability of two ...

New Delhi: The country’s top drug regulator, the Drugs Controller General of India (DCGI), has received about 1,000 applications from micro, small and medium enterprise (MSME) medicine ...

The pharmaceutical testing lab BRS Analytical Service recalled products used to relieve dry and irritated eyes after "deviations" were found in adhering to FDA safety regulations.

Compliance of Revised Schedule M guidelines has not been a major worry for large manufacturers who have been into exports, especially to the US, as they have been following US FDA specifications ...

According to the FDA's FY 2023 Annual Report, the agency conducted 2,953 inspections globally in fiscal year 2023, comprising 2,499 routine surveillance inspections and 454 for-cause inspections ...

Among these, Current Good Manufacturing Practice (CGMP) guidelines set by agencies such as the U.S. Food and Drug Administration (FDA) play a pivotal role. Pharmaceutical CGMP manufacturing ...

Revised GMP norms for small drug firms to be issued soon; to be effective December As part of the government's guidelines, which were announced in July 2023 and notified in December, drugmakers ...

GMP ICHQ7 compliance is a critical benchmark for the pharmaceutical and biotechnology industries, ensuring that products are produced consistently and abide by the highest quality standards. Oligo ...

GMP regulations provide guidelines and minimum requirements in manufacturing and development practices and facilities to ensure products are consistently safe, pure, and effective for their intended ...