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Jan 11, 2024

IVD Manufacturer Clinical Evidence Needed for IVDR Performance Evaluation Reports. Where to Begin?

IVD grouping

Jan 11, 2024

The Importance of Properly Grouping IVD Registrations Under the EU IVDR

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Jan 11, 2024

The Role of Medical Device Economic Operators in Europe

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Jan 11, 2024

How Much Postmarket Surveillance (PMS) Data Should We Have In Our Clinical Evaluation Reports (CERs)?

Jan 11, 2024

Strategy for Regulatory Compliance for MDR With Template

Jan 11, 2024

EU MDR CER and EU IVDR PER for Software: Understanding MDCG 2020-1