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Glen Emelock

Contract Lead Auditor/technical Expert at National Standards Authority of Ireland

Glen Emelock has over three decades of experience in the medical device and clinical trial sectors. Currently serving as Contract Lead Auditor and Technical Expert at the National Standards Authority of Ireland since 2003, Glen focuses on ISO 13485, EUMDD, EUIVDD, and CMDCAS assessments. As a Senior Partner at The CRO Group, Inc. since 1996, responsibilities include managing FDA-required consumer and OTC clinical trials, preparing 510(k) submissions, and establishing compliance with ISO 13485 and risk management processes. Previous roles include Director of the Medical Device Division at both TUV Product Service and TUV America, where Glen oversaw ISO assessments, and Hardware & Software Development Manager at Millipore, concentrating on drug device combination systems.

Location

Melrose, United States

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National Standards Authority of Ireland

As Ireland’s official standards body, the National Standards Authority of Ireland (NSAI) aims to inspire consumer confidence and create the infrastructure for products and services to be recognised and relied on, all over the world. NSAI is the state agency is responsible for standardisation, conformity assessment and measurement, and was established under the National Standards Authority of Ireland Act 1996. NSAI reports to the Minister for Enterprise, Trade and Employment. Contact us: info@nsai.ie | Follow NSAI Twitter @NSAI_Standards | Watch NSAI Media www.youtube.com/user/NSAImedia | Subscribe to NSAI Ezine www.nsai.ie/NSAI-Ezine


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Headquarters

Santry, Ireland

Employees

51-200

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