Latest / Medical Device made Easy Podcast
From Verification & Validation to Global Market Access | V&V, DHF & IMDRF
Developing a medical device successfully requires several pieces to work together. Manufacturers must demonstrate that the product meets its requirements, maintain reliable design documentation, and understand how regulatory expectations differ—or increasingly align—across global markets.
In this Easy Medical Device podcast collection, we explore three connected topics that represent different stages of this journey: Verification & Validation, Design History File remediation, and IMDRF and regulatory reliance.
Making Verification & Validation Practical
Verification and Validation are…
The skinny
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