A transformative approach to creating and maintaining aggregate reports. 

Authoring and updating aggregate safety reports represents one of the most time consuming and resource intensive regulatory requirements. Unfortunately, the traditional approach to creating and maintaining aggregate reports via desktop software does nothing to facilitate reuse of redundant information embedded in safety documents. Docuvera addresses the inefficiencies of traditional methods by enabling the efficient creation and maintenance of safety reports through all stages of the product lifecycle. And by reducing the burden on authors, productivity can increase.

A single platform to increase the quality and consistency of document development. 

Through an easy-to-use, component authoring interface, Docuvera facilitates single-source production and reuse of safety content across any document type. Component-based content can easily be reused to build a variety of safety content and to assemble local versions of those documents. With Docuvera, you’ll benefit from reduced time to generate and improve the quality and consistency of pharmacovigilance documentation like Reference Safety Information, Safety Update Reports, Periodic Benefit-Risk Evaluation Reports and more.

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