It’s an iterative process because risk never disappears, and products must continuously evolve to new standards.

Able Medical Devices, a Marquette-based medical device manufacturer, is expanding its operations in Michigan’s Upper ...

DCGI is planning to amend the Medical Devices Rules, 2017 to include a provision for quality requirement for non-sterile and ...

Recalled heart devices often do not go through clinical testing, a new study found, highlighting growing concerns about the ...

VitalPath Global Sales VP Nichole Ramus was previously at Vantedge Medical, Heraeus Medevio and Quality Tech Services (Cretex ...

India’s apex drug regulator is collating information on adverse events due to medical devices to take timely action against ...

The Drugs Technical Advisory Board (DTAB) has approved a proposal to amend Rules 19H and 19J of Chapter IIIB of the Medical ...

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Findings from a new survey of executives in MedTech companies reveal that the majority of their revenues come through contracts with healthcare facilities, integrated delivery networks (IDNs) and ...

The voluntary scheme, launched officially on Oct 16, will rate the devices according to their level of cyber-security ...

Learn how to effectively navigate the challenges of CMC in breakthrough drug development. Discover key strategies here.

MALAYSIA’S most promising innovators from higher education institutions are gearing up to showcase their pioneering medical ...