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Building off UL’s history of more than 120 years of safety science, UL provides comprehensive services – from advisory at product concept to post-market support, – to help medical and IVD companies manage the complex world of laser safety requirements including 21CFR Part 1040.11, IEC 60825-1 and IEC 60601. UL has offices around the world to help you meet global regulatory submissions requirements.

Our experts are active in the areas of clinical and non-clinical testing, human factors engineering, regulatory submissions, quality systems, learning management systems, electrical and mechanical engineering, software validation, wireless, EMC and cybersecurity, emerging technologies such as interoperability, wearable medical devices and home use environments. With our global offices, local expertise and
accredited test labs, UL is readily prepared to support industry innovation and regulatory needs.

Provides a brief overview of UL’s services across industries and markets.

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