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.
In 2014, the International Electro technical Commission (IEC ) published a revision of the electromagnetic compatibility (EMC) requirements for medical devices under a 4th edition of IEC 60601-1-2. These revisions include a number of changes, including new immunity and more robust risk analysis requirements. The effective date for the new standard is April 1st 2017, yet the medical device community has seen an increasing need to begin adopting these standards now, nearly two years in advance of that deadline.
Make sure you are Planning Ahead for IEC 60601-1-2 4th Edition for Medical EMC