Unencumbered Quality document development.
For pharmaceutical companies, efficiently developed and accurate Quality documents are critical in ensuring SOPs are up-to-date and available to the appropriate teams and auditors. As regulations change, so do the demands of the business to ensure compliance. Pharmaceutical companies can no longer rely on the cumbersome, error-prone systems of the past which expose them to risk of compliance failure. It’s time for a structured component authoring solution that enables efficient and accurate development of Quality documentation.
An end-to-end solution that drives efficiency.
Component authoring improves efficiency by enabling authors to reuse approved, compliant blocks of content to build and update a wide range of SOPs and Quality documents. As a single platform to author, review, approve, translate, reuse and publish Quality documents, Docuvera is an end-to-end solution that enables content owners to efficiently produce consistent and accurate SOPs and other documents.
Robust, collaborative, and easy to use
A scalable enterprise-level LCMS solution built for writers, curriculum developers, and SMEs in a collaborative environment.
Engage learners with responsive, adaptive, eLearning & microlearning
Create and manage large volumes of learning content easily and securely
Localize and translate content by the word, not the document
Reuse content within and between courses, saving time and money
Collaborate and review in real time with course developers and SMEs
Deliver interactive courses for every device with truly adaptive HTML5 publishing
Write once, publish everywhere
