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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Improving product design through task analysis

US FDA outlines next steps following COVID-19 Pandemic Recovery and Preparedness Plan (PREPP)

The EU MDR and human factors engineering (HFE) requirements for post-market surveillance (PMS)

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Argentina medical device regulatory approval process

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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

Improving product design through task analysis

US FDA outlines next steps following COVID-19 Pandemic Recovery and Preparedness Plan (PREPP)

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Related Service

The EU MDR and human factors engineering (HFE) requirements for post-market surveillance (PMS)

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?