革新的でコラボラティブ、かつ連携した新規プログラムの管理
Establish a document management and technical publishing program that generates accurate technical documents which are perfectly synchronized with product data.
Our publishing solutions for the pharmaceuticals industry allow your company to maintain organized, up-to-date configurations of re-usable authored content and data. This helps to reduce the effort required for publishing precise technical documentation while maximizing cost-effectiveness for configurations that are specific to any language, market, or product type.
Establish a document management and technical publishing program that generates accurate technical documents which are perfectly synchronized with product data.
Our publishing solutions for the pharmaceuticals industry allow your company to maintain organized, up-to-date configurations of re-usable authored content and data. This helps to reduce the effort required for publishing precise technical documentation while maximizing cost-effectiveness for configurations that are specific to any language, market, or product type.
In the pharmaceuticals industry, requirements for technical documentation authoring processes are becoming increasingly complex due to diverse markets, variations in production, unique packaging processes, and stringent, varied regulatory mandates. Technical documents supporting these specifications must be available in a variety of languages, and adhere to quality management processes necessary for compliant regulatory submissions, marketing, and distribution.
Our technical publishing solutions offer integrated digital document management that combine the power of the world’s leading global lifecycle platform with streamlined authoring and publication tools.
Utilize advanced markup capabilities to provide comments and annotations on files which are managed and captured automatically. This helps improve the timeliness and quality of pharmaceutical artwork and packaging.
Manage complex technical content at your pharmaceutical organization with change and configuration management controls. Our solutions enable cascading updates triggered by product data and production configuration changes.
Simplify and error-proof pharmaceutical document authoring and reviews by directly placing templates into workflows using familiar document tools for editing, viewing, and markup.
Manage technical documentation within a product and plant lifecycle context for the pharmaceuticals industry. Enable companies to collaborate globally and utilize geographically distributed product data, using templates and workflow automation.
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 text and illustrations as reusable content to create multiple document types and publish to different formats. Link this to content sourced from engineering information to support change impact analysis and streamlined updates at your pharmaceutical company.