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  • Services
    • Medical Device Regulatory Consulting
    • Technical Documentation for Medical Devices
    • SaMD Compliance & Software Documentation
    • External PRRC & QMR Services
    • In-Country Representation for Medical Devices & SaMD
    • Micro Consulting for MedTech & SaMD Compliance
  • Training
    • Workshops & Inhouse Training
    • Regulatory Accelerator Programs
    • Startup Office Hours
    • Our Courses
  • About us
  • Resources
  • Contact us
  • FAQs

Daily Archives: August 9, 2024

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qsr qmsr iso

Download Our Comprehensive Comparison of QSR, QMSR and ISO 13485 Requirements

Regulatory AffairsBy Anne ArndtAugust 9, 2024Leave a comment

The introduction of the Quality Management System Regulation (QMSR) by the US Food and Drug Administration (FDA) signifies a pivotal shift for medical device manufacturers. As of February 2, 2024, the QMSR updates the FDA’s Quality Management System requirements under 21 CFR part 820 to align more closely with the ISO 13485:2016 standard. With the…

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