New requirements you should know for medical EMC


Intertek EMCPlan now to ensure your medical devices comply with new EMC requirements by the December 2018 effective date.

Since the development cycle can be 2-3 years, it is important to understand the new IEC 60601-1-2 EMC 4th Edition standard now when designing medical devices. To provide you guidance on these important changes and improve your speed to market, Intertek’s industry experts developed this complimentary white paper.

The paper features detailed information on:

  • Risk Management File
  • Test planning
  • Emissions & immunity testing requirements
  • Expected global implementation roadmap

Download this paper on

DeviceTalks West: Expertise you need to know

textadimage Medical device suppliers are light years away from the days when they merely filled orders to spec for medtech OEMs – as a visit to the upcoming DeviceTalks West will quickly confirm.

From incorporating steerability into catheters to getting validation and testing done right, the companies serving the medical device industry have become specialized experts in their own right.

Read on to discover five example of medical device expertise to be had at DeviceTalks West, which runs Dec. 11–12 in Orange County, Calif.

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