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 new edition introduces new product categories, new test levels, and eliminates the “life-support” device category.
Take this opportunity to gain insight into the 4th edition and learn what you need to do to ensure compliance for your medical device and avoid loss of valuable time and revenue.
Please fill out the form below to gain access to the webinar recording.