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QA/RA Consulting, Auditing & Training

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Jan 12, 2024

MDCG 2022-6: Making Changes to Legacy Devices Without Triggering EU IVDR Compliance

Jan 12, 2024

Supplementing Your Medical Device PMS Efforts with Online Data

Jan 12, 2024

Preparing for a Notified Body Medical Device Clinical Audit

may 26

Jan 12, 2024

The New IVDR Compliance Deadline Extension Explained