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Utilization of Device Code Lists Published by IMDRF (Doc ID 2968843.1)

Last updated on SEPTEMBER 08, 2023

Applies to:

Oracle Life Sciences Argus Safety - Version 8.2.2 and later
Information in this document applies to any platform.

Goal

What was the rationale for Argus Safety recommending implementation of Device code lists published by U.S. Food and Drug Administration (FDA) rather than Device code lists made available by International Medical Device Regulators Forum (IMDRF) ?

Solution

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In this Document
Goal
Solution
References

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