docuvera: for regulated documents

A single platform to author, review, approve, translate, reuse and publish components of content to regulated documents.

The pharmaceutical industry is dependent on regulated documents to ensure compliance in a highly regulated environment. As regulations change, become more complex and diverse, so do demands on the business to ensure compliance. This makes the development and maintenance of required, regulated documents increasingly difficult. This reality has the potential to expose pharmaceutical companies to a higher risk of compliance failure.