This course is based on the 2016 version of the ISO 13485 Standard, providing skills necessary to perform internal process audits in the medical device industry. It features a detailed review of the ...

This course is based on the 2016 version of the ISO 13485 Standard, providing skills necessary to perform internal process audits in the medical device industry. It features a detailed review of the ...

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 ...

(MENAFN- ForPressRelease) Punyam is pleased to start the ISO 13485 certification consultancy for Medical Devices - Quality Management Systems. ISO 13485:2016 Medical Devices - Quality Management ...

Dublin, July 28, 2025 (GLOBE NEWSWIRE) -- The "Medical Device Single Audit Programme (MDSAP) Training Course" has been added to ResearchAndMarkets.com's offering. The Medical Device Single Audit ...

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, ...