Argentina medical device & IVD approval process

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Within the UL family of companies we provide a broad portfolio of offerings to all the medical device industries. This includes certification, Notified Body and consultancy services. In order to protect and prevent any conflict of interest, perception of conflict of interest and protection of both our brand and our customers brands, UL is unable to provide consultancy services to Notified Body or MDSAP customers. UL has processes in place to identify and manage any potential conflicts of interest and maintain impartiality.

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In brief: China NMPA seeks feedback on optimization of medical device standards

New guidelines published on integrating UDI into quality management systems under MDR, IVDR in Europe

Countdown to IVDR Date of Application – Key Requirements and Challenges

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Argentina medical device regulatory approval process

Questions? Request more information from our specialists

Have questions on what Emergo can do for you?

© 2021 EMERGO by UL. All Rights Reserved. Privacy Terms of Use Data Subject Access Request Portal

In brief: China NMPA seeks feedback on optimization of medical device standards

New guidelines published on integrating UDI into quality management systems under MDR, IVDR in Europe

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Related Service

Countdown to IVDR Date of Application – Key Requirements and Challenges

Argentina medical device regulatory approval process

Questions? Request more information from our specialists

Related

Argentina medical device regulatory approval process

Have questions on what Emergo can do for you?