Learn from industry practitioners and experts why implementing an FDA 21 CFR Part 11 Software System is so essential. Within a year of 21 CFR Part 11 first going into effect MasterControl Inc. introduced the industry’s first document management software solution specifically designed to help life sciences organizations comply with FDA regulations, the regulations delineated in 21 CFR Part 11 in particular. Master Control’s solutions streamline and automate GxP processes and facilitate effective management of document control, change control, training control, audits, corrective/preventative action (CAPA), customer complaints, and other quality and business processes, all under a single Web-based platform. MasterControl GxP process management software solutions go beyond FDA 21 CFR Part 11 requirements and regulations to help companies also sustain current industry best practices (CGxP). Since then, MasterControl has continued to go beyond requirements for implementing a GxP process management software solution for easier compliance, faster validation, and better CGxP process management.
