DUBLIN--(BUSINESS WIRE)--The "Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation" training has been added to ResearchAndMarkets.com's offering. The new medical device regulation EU MDR ...
The European Commission adopted Implementing Decisions (EU) 2022/6 of 4 January 2022 and 2022/15 of 6 January 2022 regarding harmonised standards in support of Regulation (EU) 2017/745 (the "Medical ...
Introduces early stage audit readiness solutions to streamline ISO 13485 certification for medical device and IVD companies inline with MDR, IVDR and FDA QMSR CHARLOTTE, NC, UNITED STATES, April 29, ...
DUBLIN--(BUSINESS WIRE)--The "Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation" conference has been added to ResearchAndMarkets.com's offering. The new medical device regulation EU MDR ...
LONDON, UK; 15 June, 2022 – Allmed Medical GmbH, part of Allmed Group (“Allmed” or “the Company”), a producer of end-to-end haemodialysis solutions, today announces that it has received Medical Device ...
ZAVENTEM, Belgium, May 20, 2025 (GLOBE NEWSWIRE) -- SYNDEO Medical, a Belgian-based developer of interventional procedure solutions, is pleased to announce that it has received ISO 13485 certification ...
DONGGUAN, GUANGDONG, CHINA, January 13, 2026 /EINPresswire.com/ — As healthcare moves toward proactive and at-home wellness management, industry leaders are coming ...
DONGGUAN, GUANGDONG, CHINA, January 15, 2026 /EINPresswire.com/ — As European populations continue to struggle with sleep disorders such as obstructive sleep apnea ...
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