Technical Publishing for Medical Devices

Technical Publishing for Medical Devices

Increasingly stringent governmental regulations, complex products, and customized user specifications around the globe are affecting delivery, cost, and quality control processes for labeling in the medical device industry. 

Our technical publishing solutions for medical instruments and equipment deliver a competitive advantage through comprehensive and accurate technical document authoring and lifecycle management of labeling content by enabling direct usage of engineering source data.

Increasingly stringent governmental regulations, complex products, and customized user specifications around the globe are affecting delivery, cost, and quality control processes for labeling in the medical device industry. 

Our technical publishing solutions for medical instruments and equipment deliver a competitive advantage through comprehensive and accurate technical document authoring and lifecycle management of labeling content by enabling direct usage of engineering source data.

Technical_Publishing for Medical Devices

Learn More

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 the region, governing authority and language, as well as the unique processes involved. Companies must produce a variety of electronic and printed labeling publications which incorporate information in their system.

Our solutions offer an integrated and complete technical publishing platform for labeling and the management and authoring of lifecycle content such as instructions for use (IFU) and service manuals. This combination of the leading global PLM platform with accurate, simplified product and process management tools ensures best-in-class practices and results at your med-tech firm.

Technical_Publishing for Medical Devices

Funzionalità della soluzione

Artwork Design & Proofing

Utilize advanced markup capabilities for file comments and annotations which are automatically managed and captured.  By collaborating on artwork and proofing within the lifecycle, your company can improve the timeliness and quality of device artwork and packaging.

Bill of Materials Management

Manage engineering BOM definitions - from simple CAD structures to complex product definitions - across globally distributed design teams. Create multiple product configurations using multi-CAD design data stored anywhere.

Document Authoring Tool Integrations

Enable the authoring and editing of medical device labeling content using templates placed directly into creative or review workflows. Working in a familiar environment encourages simplified and widespread collaboration.

PLM Platform

Manage technical documentation within the product lifecycle context. This enables your medical device company to collaborate and comprehensively access real-time production data.

RapidAuthor Interactive Visual Content

Le pubblicazioni tecniche altamente descrittive possono essere molto proficue, soprattutto se aiutano i team di produzione e assistenza ad aumentare la produttività. RapidAuthor per Teamcenter estende il tuo investimento in dati di progettazione, consentendoti di riutilizzare tali contenuti direttamente nella documentazione tecnica. I contenuti XML CAD e PLM vengono convertiti direttamente in testo oppure in grafica e animazioni 2D/3D, per consentire ai clienti di farsi un'idea più precisa del funzionamento dei prodotti e delle decisioni da prendere per fabbricarli e fornire assistenza.

Structured Content Management

Manage medical device text and technical illustrations as components to reuse in multiple documents and then publish automatically to various formats. This provides greater compliance with regulatory guidelines and organizational requirements.

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