Dublin, Feb. 25, 2026 (GLOBE NEWSWIRE) -- The "Process Validation for Medical Devices Training Course (June 4th - June 5th, 2026)" training has been added to ResearchAndMarkets.com's offering. This ...

New process device profiles have been added by ODVA to the EtherNet/IP specification to provide end users with another tool to help optimize plant operations. According to ODVA, the new process device ...

WALDWICK, N.J.--(BUSINESS WIRE)--NextPhase Medical Devices LLC, a leading provider of electronic manufacturing services (EMS) and single-use disposable devices to leading medical device OEMs, recently ...

As noted in Chapter 1, the committee was charged by the Food and Drug Administration (FDA) to review the 510(k) clearance process and answer two principal questions: Does the current 510(k) clearance ...

At the SPS 2024 event Nuremberg, Germany, ODVA announced two new updates for EtherNet/IP. The first announcement relates to the enhancement of CIP Safety on EtherNet/IP to allow for the use of ...

Staying inside increasingly narrow process windows as specialty devices scale, diversify, and enter high-volume production.

BOSTON--(BUSINESS WIRE)--908 Devices Inc., (Nasdaq: MASS), a pioneer of purpose-built handheld and desktop devices for chemical and biochemical analysis, announced that National Resilience, Inc.

Sponsors of medical devices now have a new process to apply for a certificate of free sale or an export certificate in Australia, the Therapeutic Goods Administration (TGA) announced Tuesday. “Some ...

(MENAFN- GlobeNewsWire - Nasdaq) Key market opportunities include enhancing regulatory compliance for medical devices through process validation. Understanding quality management ties, FDA/EU/UK ...

Prior to the Medical Device Amendments (MDA) of 1976, medical devices generally had not undergone premarket review by the US Food and Drug Administration (FDA). The MDA created three classes of device ...