Video: European Union Medical Device Regulation Compliance Using Informatica Axon

As of 26 May 2020, the MDR lays down rules concerning the placing on the market, making available on the market or putting into service of medical devices for human use and accessories for such devices in the European Union. The MDR also applies to clinical investigations concerning such medical devices and accessories conducted in the European Union.

Join us in learning how Informatica Axon can be used for the European Medical Device Regulation Compliance.

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