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4.5 ★★★★★ 47 Reviews
FDA QMSR FDA QSR 21 CFR 820 ISO 13485 Medical Devices

ISO 13485 and FDA QSR 21 CFR Part 820 Requirements

12hrs
CQI-IRCA Certified Course

ISO 13485 and FDA QSR 21 CFR Part 820 Requirements is for Practitioners & Auditors who want to understand the requirements, including similarities, differences and key aspects of both the ISO 13485 standard and the FDA Quality System Regulation (QSR 21 CFR Part 820).

4.4 ★★★★★ 10 Reviews
FDA QMSR FDA QSR 21 CFR 820 Medical Devices

Introduction to FDA QMSR Training

45mins

Introduction to FDA QMSR Training is for individuals or organizations looking for a concise, high-level introduction to the FDA’s Quality Management System Regulation (QMSR).

WHAT'S NEW

2025 Training Guide

Transformational Training for ISO Standards, Auditing & Medtech QA/RA

2025 Training Guide

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Our team has you covered with expert insights & updates to stay on top of the latest updates, trends, and changes in the industry.

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Comply Guru is now an Approved Provider with the Regulatory Affairs Professionals Society (RAPS) offering more recognition for our Medical Device Trai...
New Courses to Reach New Heights in 2025
Eoin discusses the exciting new courses Comply Guru has launched in 2025 for QARA Professionals within MedTech....
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