FDA Guidance on Design Validation
FDA Guidance on Design Validation
Oct 1, 2021
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LAST CHANCE TO REGISTER! Are you a software engineer looking to align your product with global healthcare standards? We’re offering a 3-day MDSV course (February 10-12, 2026) that’ll speed you ahead in the evolving world of medical device software. Through a mix of lectures and real-world case studies, you’ll learn to: ✅ Apply key laws, regulations, and standards (21CFR820, ISO 13485, ANSI/AAMI/IEC 62304, ISO 14971, and more) ✅ Understand software classification and related validation activities
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