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Are you ready for the new FDA Quality Management System Regulation (QMSR)? We’re offering our flagship QMSR course, Navigating and Implementing the Requirements: March 16-20, 9:00am–6:00pm EST (final day ends at 1:00pm). We'll help you apply the FDA’s amended 21 CFR 820 and ISO 13485:2016 and give you tools to achieve full compliance before next year. You’ll learn to: ⚙️ Implement a Risk-Based QMS 📘 Align with ISO 13485:2016 🧭Ensure 2026 Compliance 💡 Apply QMSR in Practice Developed by FDA-le
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Are you ready for the new FDA Quality Management System Regu…
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Heading to Dublin? AAMI’s flagship QMSR training is coming to Ireland this February. This and more in the first learning lineup of 2026! Mastering HTM Accreditation Compliance: Stress Less, Achieve More Jan 27 & 29, 2026 | Virtual | 1–3 PM ET Learn how to meet HTM compliance requirements with less stress and more confidence. Understand Joint Commission updates, AEM best practices, and strategies for survey readiness. Integrating Risk Management into the Product Life Cycle Feb 4–6, 2026 | Virtual
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Heading to Dublin? AAMI’s flagship QMSR training is coming to Irelan…
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AAMI’s Quality Systems Foundation course is the perfect introduction (or refresher!) on medical devices and the FDA’s quality system requirements! We’re offering a virtual, two-day program January 21-22, 2026, 11:00am-3:00pm EST. Learn the fundamentals of FDA’s Quality System Regulation and ISO 13485:2016, which will be incorporated into the upcoming Quality Management System Regulation (QMSR). Whether you’re new to the field or an industry veteran seeking a refresher, this course delivers the t
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AAMI’s Quality Systems Foundation course is the perfect introduction …
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Aviation Quality Management System (QMS) - AVISAV
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A Comparative Intro to Medical Device & Pharmaceutical Regulations | April 6–7, 2026 (Virtual) This introductory Expert Insights training provides a clear side-by-side look at FDA medical device and pharmaceutical regulations, helping you understand where they differ, where they overlap, and how to interpret key requirements. You’ll explore QMSR vs. 21 CFR 210/211, learn essential terminology, and get a brief introduction to combination products—through interactive material, quizzes, polling, an
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