The need and opportunity for managing records and regulatory submissions electronically, has never been so great in the pharmaceutical industry. This poses great challenges for business process, for industry standards and for related technologies so as to ensure quality and compliance over the full lifecycle of information management.

Whether your organisation is entering electronic information management for the first time, optimising established processes and systems or pushing the boundaries of document and content management, it is vital for decision making within business to be based on up-to-date information concerning industry and technological standards, and on current Regulatory Agency expectations and the industry's response.