Component authoring for Life Sciences.
Docuvera’s component authoring improves efficiency and compliance by enabling the ability to reuse approved, compliant blocks of content within and across clinical, regulatory, medical, safety, CMC and other documents. Author, review and update once – reuse across multiple documents. Docuvera’s simple user experience enables a seamless transition for medical authors upgrading from desktop publishing software.
A powerful and easy-to-use service in one intuitive platform.
The Docuvera platform combines an intuitive web interface with the latest web technologies to provide a powerful, yet easy-to-use service that relieves the pain of traditional document creation.
A single platform to author, review, approve, translate, and publish regulated documents by reusing approved, compliant component content.
Component authoring made simple
Authors can easily reuse approved blocks of content to assemble documents. No technical expertise or expensive support required.
Intelligent component reuse
When your content is created as structured components, it can be reused across multiple documents, by as many authors and contributors as needed. No more wasted time continuously copying and pasting or creating content from scratch.
Seamless propagation of modified content
Docuvera notifies authors immediately when source content changes and gives them the opportunity to review and accept those changes into their document. No delays or confusing back and forth between content developers.
Collaborative web review and approval
Cross-department review of documents can happen collaboratively in a single forum for discussions and resolutions. No more manual merging of Word track changes.
Omni-channel document publishing from the same project
Create Word, PDF, HTML and other documents from the same project by applying different styles during the publishing process. No need to manually create different document types.
How does it work?
- The simple, drag and drop interface allows authors to easily reuse pre-approved component content to assemble new documents.
- Collaborative workflows allow users to simultaneously contribute to authoring, review, and approval of documents.
- Word, PDF, HTML and other document types are published from the same project, but with each document type having a specific set of styles and layout.
- Changes to reused component content seamless propagate to documents where information is reused. Local authors can review source changes and incorporate updates as necessary.
- A clear audit trail of document and component modifications, workflows and published documents is stored in the system for compliance and quality purposes.
Authoring, collaboration, reuse and publishing
right at your fingertips.
Long gone are the days of time wasted on locating and updating multiple documents stored in silos. With Author-it, any object – be it a word, phrase, or paragraph – can easily be changed in one place and pushed out to multiple publishing outputs simultaneously. No more copy and paste!
Docuvera solutions
Choose the solution that’s right for you.
Clinical
Docuvera brings efficient and easy-to-use component-based authoring capabilities to the creation of and revision process for pre-clinical and clinical content.
Global Labeling
Docuvera’s end-to-end solution reduces labeling content production times, ensures alignment to compliant content, and creates faster time-to-market for regulatory submissions.
Medical Information
Docuvera reduces medinfo content production times and enables omnichannel distribution of medical content to Health Care Professionals.
Chemical Manufacturing and Controls
Docuvera enables the efficient creation and maintenance of CMC documentation by reusing core component content to assemble local documentation.
Chemical Manufacturing and Controls
Docuvera enables the efficient creation and maintenance of CMC documentation by reusing core component content to assemble local documentation.
Aggregate Reporting and Safety Writing
Docuvera brings component-based reuse to the creation and maintenance of aggregate safety reports for all stages of the product lifecycle.
Quality Documents/SOPs
Review, approve, translate, reuse and publish quality documents and reuse approved content components to efficiently assemble accurate SOPs with Docuvera.
Technical Publications, Training and eLearning
Our sister solution, Author-it, enables authors to create, collaborate, manage, reuse, publish and translate documentation – all in one platform.