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IVDR Overview White Paper
White paper

IVDR Overview

Explore the In Vitro Diagnostic scope and definitions as well as the manufacturer requirements

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Reprocessing Validations for Reusable Medical Devices
Webinar

Reprocessing Validations for Reusable Medical Devices

Learn about sterilization requirements for reusable medical devices

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ISO 13485:2016 Revision
Report

ISO 13485:2016 Revision Fact Sheet

A quick guide to the revised ISO 13485:2016 standard

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