Reduce complexity of clinical documentation creation, and speed time to market.
Clinical trial documents are complex, and their creation is an essential part of bringing products to market. The traditional approach to authoring and managing clinical information via desktop software is no longer sustainable to meet the critical timelines for their development.
Docuvera brings component-based reuse to create and update pre-clinical and clinical content. Unrestricted by content silos, the service facilitates single source production and reuse of clinical content to vastly improve the efficiency in developing protocols, CSRs, and other clinical documents.
Ease the burden on your authors, minimize errors and compliance headaches.
Long clinical development cycles, regulatory and ethics requirements and the high cost of rework ensures that clinical documentation is the focus of heavy scrutiny. Within the Clinical area, numerous documents are created to support a clinical trial and content is frequently reused across documents. Docuvera reduces the burden on authors by facilitating reuse of information across documents, which also minimizes the possibility of errors and ensures compliance.
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
