Webinar: How To Prepare For FDA Migration To ISO 13485 And MDSAP

[fa icon="calendar'] Mon, May 06, 2019 / by David Bolton

 

Media theorist Marshall McLuhan may not have had quality management for medical devices in mind when he coined the phrase “global village” in the 1960’s, but the fundamental interconnectedness of modern society has brought his concept to life. And while technology is at its core, the need for international harmony in the regulatory sphere is arguably a key QMS issue.

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Medical Devices ISO Standards Life Sciences Regulatory Compliance iso 13485

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