Fake ISO certificates claiming safety and quality of medical devices need to be verified: Experts: Shardul Nautiyal, Mumbai Thursday, January 15, 2026, 08:00 Hrs [IST] Experts hav ...

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 ...

Dublin, June 28, 2024 (GLOBE NEWSWIRE) -- The "The US FDA QMSR Transition - 21 CFR 820 and ISO 13485" training has been added to ResearchAndMarkets.com's offering. The US FDA, after years of ...

San Diego, CA, June 01, 2020 (GLOBE NEWSWIRE) -- MadTranslations, the industry-leading translation and localization services arm of MadCap Software, Inc., today announced that it has achieved ...

The medical device sector must meet stringent regulatory requirements plus convince potential customers that they make reliable, safe products. Having a strong commitment to quality can help customers ...

DUBLIN--(BUSINESS WIRE)--The "An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices Training Course (Nov 20, 2025)" training has been added to ResearchAndMarkets.com ...

South African Health Products Regulatory Agency (Sahpra) has indicated that ISO 13485 certification is a prerequisite for the application or renewal of a medical-device license, with effect from 1 ...

New generations of small medical electronics devices demand the highest levels of quality and reliability For EMS providers and contract manufacturers, the International Standards Organization (ISO) ...

Hoggan Scientific, LLC, a globally recognized leader in the design and manufacture of medical devices, is proud to announce that it has successfully received recertification for ISO 13485:2016, the ...

PLEASANTON, Calif.--(BUSINESS WIRE)--Boyd Corporation, a global leader in sealing, protection and thermal management solutions, announced their facility in Chonburi, Thailand has achieved ...