Enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes.
Evaluating how your products and services meet and exceed quality, safety, sustainability and performance standards.
Validating the specifications, value and safety of your raw materials, products and assets.
The fourth edition of IEC 60601-1-2 has been approved, and this means dramatic changes for the medical device industry. This edition introduces new product categories, new test levels, and eliminates the “life-support” device category.
This free webinar on IEC 60601-1-2 4th Edition will help you gain a better understanding of:
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