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Did you know that additional EMC compliance regulations exist for advanced diagnostic medical equipment? The life sciences technology industry has seen rapid growth since the completion of the human genome sequencing in 2001. Targeted disease research requires more advanced medical equipment, such as In-Vitro Diagnostic (IVD) equipment.

IVD devices shall function properly and safely in home environments, as well as in typical healthcare environments (hospitals, clinics, doctor’s offices).

Download the whitepaper “Life Sciences EMC Requirements for CE Marking” to learn about performance criteria for immunity tests, compliance revisions on the horizon, user’s manual instructions & warnings, and more!

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Life Sciences EMC Requirements for CE Marking