With global health and regulatory authorities continuing to push for tighter regulations surrounding disclosure and e-standards, life sciences companies are increasingly challenged by fragmented, paper-based processes and out-of-date technology systems.

How inefficient is regulatory information management in life sciences organizations?

New research by IDC Health Insights states that the cost of bringing new drugs to market ranges from $800 million to $1.2 billion, and estimates that roughly a quarter of the cost comes from the content requirements associated with working in a regulatory compliant environment.

Join Pharmaceutical Executive Magazine and leading analyst Dr. Alan Louie of IDC Health Insights for a complimentary webinar titled “Managing Paper at Its Roots: MovingBeyond Document Management to Enterprise Content Compliance.”

This webinar will examine the growing trend in the life sciences industry away from traditional document management systems to emerging Enterprise Content Compliance (ECC) solutions. You’ll learn how ECC solutions are changing and accelerating traditional regulatory document preparation by allowing companies to compress the time spent authoring and reviewing content for protocols, submissions, labeling, clinical trial disclosure, and other mandates.

Register today to receive your complimentary copy of IDC Health Insights’ report titled “Managing Paper at Its Roots: MovingBeyond Document Management to Enterprise Content Compliance.”