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Medical Device Non-Product Software Validation

Jan 12, 2024

Medical Device Production, QMS and NPS Software Risk Assessment, Validation, and Protocols

Jan 12, 2024

ISO 14971 and the Basics of Medical Device Risk Management Explained

paper checklist with a black leaded pencil

Jan 12, 2024

25 EU MDR Articles That Apply to Legacy MDD Medical Devices Right NOW

Jan 12, 2024

Pharma Process Validation: Where Do We Start?

Jan 12, 2024

Drug, Device, or Both? Overview of FDA Premarket Regulation of Combination Products

Jan 12, 2024

Medical Device & IVD Usability Testing and FDA Human Factors Requirements