Quality Document Control

Learn How to Automate Quality Document Control to Comply with FDA Regulations and ISO Standards

Both FDA regulations and ISO quality standards require companies to establish a system for document control that is electronic in order to ensure product quality and safety.

A document control software system ensures that production processes are all pre-approved, and that changes are restricted to authorized personnel and tracked for future review. Despite the importance of quality document control and document management, many companies continue to rely on paper-based or partially electronic system for document control. These systems are plagued by inefficiency and errors that could cause FDA-483 citations or ISO nonconformance.

Automating Document Control Processes to Comply With FDA and ISO Requirements