January 13, 2026 - PRESSADVANTAGE - In the highly regulated field of medical device labeling translation, ensuring that ...
On February 2, 2024, the US Food and Drug Administration (FDA) published a much-awaited final rule: the Quality Management System Regulation (QMSR). 1 By issuing this rule, FDA amended the medical ...
New capability delivers end-to-end traceability across all product development data, connecting milestones, decisions, and evidence across every phase of the medical device lifecycle.
Medical Device Network on MSN
The medical device manufacturing crunch
With Covid accelerating time-to-market for medical devices, digital tools play a key role in managing converging priorities ...
Engineers could avoid expensive redesigns by planning medical device testing early in development with expert guidance.
As cybersecurity threats have become more and more pressing in the healthcare industry in the last several years, FDA has taken several steps to strengthen the security of medical devices seeking ...
On Friday 21st October 2022, the Medicines and Healthcare Products Regulatory Agency (MHRA) wrote to the medical device industry to explain its intention: To extend the current standstill period by ...
HARTSVILLE, SC - January 28, 2026 - PRESSADVANTAGE - Hogge Precision Parts Co., Inc. announces enhanced capabilities in ...
STEMart announces the expansion of its genetic toxicology capabilities with the In Vivo Rat Micronucleus Test services.
The evolution of medical-grade thermoplastic polyurethanes (TPUs) continues to reshape possibilities for device manufacturers seeking materials that combine flexibility, durability and ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results