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ISO 13485 Requirements and Medical Device Audits

By Vadim MaliiUncategorized

ISO 13485 Requirements and Audits: “What’s the Best Way of Doing This?” Align with the Latest Version of ISO 13485...

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February 9, 2023

The Guide to Mastering Medical Device Risk Management

By Rick L'AmieFeatured: Regulatory Affairs, Quality Systems, Regulatory Affairs, Safety, Uncategorized

Author: Silas Minnick, Senior Quality Engineering Consultant Are you preventing risk or vulnerable to it? Whether you are a medical...

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September 1, 2020

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Consultants See Busier FDA — And More Business For Themselves

By awdesignUncategorized

Three years ago, Anne Wilson only had three staff members at QA Consulting Inc., a firm based in Austin, TX….

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November 25, 2012

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