Device Master Record Management

Device Master Record Management provides a single, integrated system to manage all elements of the Device Master Record (DMR) within accordance of the U.S. Food and Drug Administration's (FDA's) Quality System Regulation (QSR) and ISO standards. It provides full audit trails and powerful authentication controls for FDA Part 11 compliance. Device Master Record Management manages communication and process collaboration between design engineers, manufacturing engineers and software engineers from your company's globally dispersed product development teams and suppliers.

Device Master Record Management requires Engineering BOM Management.

Administrators are typically responsible for installing, upgrading, and supporting the app, as well as configuring properties and other settings in response to user and business requirements. This guide includes topics and tasks intended for administrators.

Administrators can use these resources for additional assistance available in the SUPPORT menu at http://www.3ds.com/support/documentation:

  • The Program Directory is a website that organizes all the release information for all Dassault Systemes apps for a given release. It contains information about prerequisites, installation, licensing, product enhancements, general issues, open issues, user assistance addenda, and closed issues.
  • The Knowledge Base provides question-and-answer articles for a wide range of content. You can search the Knowledge Base for issues relevant to your app.

Important: Published examples, including but not limited to scripts, programs, and related items, are intended to provide some assistance to customers by example. They are for demonstration purposes only. It does not imply an obligation to provide examples for every published platform, or for every potential permutation of platforms/products/versions/etc.

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