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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FDA asks COVID test makers to switch from emergency to premarket approvals

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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

FDA asks COVID test makers to switch from emergency to premarket approvals

Singapore’s HSA to commence Phase I implementation of UDI labeling in November 2022

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Related Service

Software as a Medical Device (SaMD): EU/US Regulatory Considerations

Scaling and Conducting Use-Related Risk Analysis (URRA)

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?