A 15 Minute Guide To Efficient And Compliant Management Of GMP Controlled Documents

Life Sciences quality and manufacturing organizations face three critical industry forces: increasingly stringent regulation; globalization; and virtualization of supply networks. These trends, along with changing user preferences, create new challenges for compliant document management including increased complexity and the need for collaboration.

This 15-Minute guide provides a short overview of these trends, and describes three best practices for improving document management practices while improving the productivity of manufacturing organization:

• Unify document management policies, processes, and systems
• Simplify user interfaces and ongoing process and system administration
• Automate document management tasks and reporting