Industry consultant Michael Drues will discuss how medical device companies can better prepare for FDA inspections.

In 2025, the U.S. Food and Drug Administration (FDA or the Agency) issued a surprising number of enforcement letters to ...

Pakistan has a total of 12 drug testing laboratories, six of which are accredited by the World Health Organization (WHO), making their test results internationally recognized. Parliamentary Secretary ...

Pakistan’s drug regulator says digital reforms at DRAP have accelerated medicine approvals and improved access to quality ...

DONGGUAN, GUANGDONG, CHINA, January 13, 2026 /EINPresswire.com/ -- Globally, the medical device industry is changing ...

The U.S. Food and Drug Administration may soon convert an entire generation of U.S. children, especially children in foster ...

In response to global scrutiny, the Indian government will likely announce plans to set up new drug testing labs and increase ...

Nicknamed "gas station heroin," kratom has split lawmakers between those calling for prohibition and those warning regulation ...

Stringent food safety regulations will inspire innovation in machinery standards while encouraging dairy manufacturers to ...

Stability is a critical factor in drug formulation, with implications for product quality, lifecycle management, and ...

ATH-063 is a novel, oral, first-in-class, small molecule therapeutic targeting both inflammation and direct mucosal healing in patients with ulcerative colitis and Crohn's disease LOS ANGELES, CA / ...

January 13, 2026 - PRESSADVANTAGE - In the highly regulated field of medical device labeling translation, ensuring that ...