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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IVDR watch: New guidance from European MDCG ahead of date of application

IVDR Watch: European regulators add ISO 14971 to harmonized standards list

Clinical data and post-market compliance under the MDR

Applying HFE expertise early in the medical product development process

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Argentina medical device regulatory approval process

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© 2022 EMERGO by UL. All Rights Reserved. Privacy Terms of Use Data Subject Access Request Portal

IVDR watch: New guidance from European MDCG ahead of date of application

IVDR Watch: European regulators add ISO 14971 to harmonized standards list

Types

Related Service

Clinical data and post-market compliance under the MDR

Applying HFE expertise early in the medical product development process

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?