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.
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.
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.
Manage technical documentation within the context of product change and configuration management. By doing so, it links to content with engineering data, enabling significant change impact and accurate update analysis.
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.
Manage technical documentation within the product lifecycle context. This enables your medical device company to collaborate and comprehensively access real-time production data.
高度に記述的な技術文書は、それによって製造およびサービスチームの生産性が向上する場合は特に、非常に有益なことがあります。RapidAuthor for Teamcenterを使用すると、エンジニアリング設計データのコンテンツを技術ドキュメントで直接再利用できるので、その投資が無駄になりません。CADおよびPLM XMLのコンテンツは、テキストと2D/3Dグラフィックおよびアニメーションに直接変換されるため、製品の仕組みと、製品の製造とサービスを行うのに必要な決定事項をよりよく理解できます。
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.
