White Paper

Regulated Content Management and the Digital Revolution In The LIfe Sciences Industry

Source: Medidata Solutions

Globalization of clinical trials, tightening regulatory requirements, a more competitive and collaborative commercial environment, and an increasingly mobile workforce requires life-sciences companies to standardize and improve regulated content management processes to ensure information is shared with the right people at the right time.

Digitization, enabled by cloud computing, opens the way for life sciences companies to streamline the way they work and the way they gather, store, and share content. Simplicity, efficiency, and harmonization are keys to sustainable and successful content management. However, the complex nature of the clinical trial process means that sponsor companies and CROs have multiple technology solutions in play to handle activities such as working with sites, recruiting patients, monitoring trial data, managing consent forms, and interfacing with the regulators.