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Introduction to US FDA Quality Management System Regulation (QMSR) and 21 CFR 820 (QSR) Training

Sun, 02 Feb

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Virtual Event

Master FDA Compliance: Get to know QMSR - the new regulation effective Feb 2026 and current 21 CFR 820! Explore the essentials of quality management in medical devices, ensuring seamless adherence to FDA regulations. Elevate your expertise and advance your career in a comprehensive session!

Introduction to US FDA Quality Management System Regulation (QMSR) and 21 CFR 820 (QSR) Training
Introduction to US FDA Quality Management System Regulation (QMSR) and 21 CFR 820 (QSR) Training

Time & Location

02 Feb 2025, 9:30 am – 1:00 pm GMT+2

Virtual Event

About the event

The new US FDA Quality Management System Regulation (QMSR) is going to be effective on February 2026. This new regulation integrate the current QSR under 21 CFR 820 with the ISO-13485:2016 - the standard for Medical devices — Quality management systems.

The QMSR is designed to help ensure that medical devices are designed, manufactured, and distributed in a safe and effective manner.

In the training, I will emphasize the new QMSR Requirements as well as the current requirements under 21 CFR 820.


Training content:

  • Introduction to QMSR - structure and requirements

  • Comparison between US FDA QSR, QMSR and ISO-13485


Tickets

  • General Ticket

    ₪400.00
    Tax: +₪72.00 VAT

Total

₪0.00

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