The Drug Regulatory Authority of Pakistan (DRAP) has unveiled a report highlighting a significant 34 percent increase in ...

The U.S. FDA’s Jan. 14 webinar for the new Quality Management System Regulation included some fairly predictable content, but one member of the FDA staff mentioned that the agency now expects ...

DONGGUAN, GUANGDONG, CHINA, January 13, 2026 /EINPresswire.com/ -- As healthcare moves toward proactive and at-home ...

Generative AI in medtech raises questions on safety, validation, and regulatory challenges, explored in MD&M West's "GenMLP" ...

The FDA’s Center for Devices and Radiological Health has withdrawn its December 2017 final guidance for clinical evaluation ...

The FDA has approved ProlivRx, the first prescription, home-based brain neuromodulation therapy, as an adjunctive treatment ...

Lord’s Mark Industries Ltd has secured US FDA registrations for 153 orthosurgical products, enhancing India's status in global medical manufacturing.

In April, the US Food & Drug Administration (FDA) announced its decision to phase out animal testing requirements for ...

MGS, a provider of end-to-end healthcare solutions, has launched the A.i.r. Platform, a customizable auto-injector platform ...

Industry Trends and Wellness Market Expansion The retail wellness market is currently experiencing an astounding ...

IPC registers 44 small-scale medtech firms under ADRMS for reporting medical devices related SAEs: Shardul Nautiyal, Mumbai Friday, January 16, 2026, 08:00 Hrs [IST] The Indian Ph ...

The Delaware Supreme Court has partially reversed a decision ordering Johnson & Johnson to pay former Auris Health ...