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Implement and monitor regulatory compliance with SAP MDG

Unique Device Identification (UDI) is a new regulatory requirement by the US Food and Drug Agency (FDA). Starting from Sept. 2014 information about medical devices sold on the US market need to be registered in the Global Unique Device Identification Database (GUDID) from FDA.

To ensure compliance with this new regulatory requirement we have custom developed a tool for data collection, verification and submission to the FDA for a global medical device manufacturer in SAP MDG.

Target audience

This webinar gives an overview about MDG in the FDA regulation area in health care.

Objective

An exemplary implementation of the new FDA regulation "UDI" in health care with SAP MDG.

Basic information

Partner/customer

Infosys Lodestone

Instructor(s)

Alexander Meier
Principal
Infosys Lodestone

Recording

Available media

Download Media




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