Docuvera Clinical improves quality and compliance of clinical operations
Clinical trial documents are complex, yet their creation represents a series of essential steps in bringing products to market. Numerous documents are created to support a clinical trial and content is frequently reused across the set of pre-clinical and clinical documents. Long clinical development cycles, regulatory and ethics requirements and the high cost of rework ensures that clinical documentation is the focus of heavy scrutiny. However, the traditional approach to authoring and managing clinical information via a document metaphor does nothing to reduce the burden on authors or facilitate reuse of information across documents.