IEC 60601-1 Medical device equipment/medical electrical equipment. IEC 60601-1 is the standard requirement for the commercialization of electrical medical equipment in many countries.
Title 47, Part 15 is a part of title 47 of the Code of Federal Regulations (CFR) and regulates everything from spurious emissions to unlicensed low-power broadcasting. Nearly every electronics device sold inside of the United States radiates unintentional emissions and must be reviewed to comply with Part 15 before it can be advertised or sold in the United States.
C63.18-1997 – American National Standard Recommended Practice for an On-Site, AD HOC test Method for estimating radiated electromagnetic immunity of medical devices specific to radio frequency transmitters.
IEEE 1900.2 Working Group on recommended practice for the analysis of in-band and adjacent band interference and co-existence between radio systems
