Aerospace & Defense
Innovation and collaborative, synchronized program management for new programs
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Manage technical documentation within a product and plant lifecycle context. This enables your medical device company to collaborate and comprehensively access real time product lifecycle data.
Manage technical documentation within the context of product change and configuration management. Doing so links content with engineering data, enabling significant change impact and accurate update analysis.
Enable authoring and editing of medical device labeling content using Microsoft Office templates placed directly into creative or review workflows. Working in a familiar Office environment encourages widespread and simplified collaboration.
Author and illustrate medical device labeling content using engineering source data. This allows for accurate authoring of labeling content that reuses 2D & 3D device models to create informative graphic illustrations and animations.
Manage medical device text and technical illustrations as components to reuse in multiple documents and publish automatically to various formats. This allows for greater compliance with regulatory guidelines and organizational requirements.
In the medical device industry, labeling requirements are becoming increasingly complex due to stringent regulations stemming from both end-customer needs and governmental oversight bodies. For compliant product delivery, labeling must vary according to region, governing authority and language as well as unique processes involved. Companies must produce a variety of electronic and printed labeling publications which incorporate information in their system.
We offer integrated and complete technical publishing solutions for authoring and lifecycle management of labeling content, such as instructions for use (IFU) and service manuals, combining the power of the leading global PLM platform with accurate, simplified product and process management tools.