The main purpose of a regulatory information management system is to support the regulatory approval process of pharmaceutical products and/or devices.

NNIT has worked with regulatory information management systems for more than a decade, providing consulting and systems implementation services for regulatory affairs.

Consulting and implementation from NNIT give you:

• Improved operational efficiency
• Improved ability to release batches on consolidated and reliable data
• Improved operational efficiency in batch allocation, batch release, and Regulatory Affairs
• Track information on regulatory status
• Improved functionality to handle regulatory information for drug products and devices for all markets
• Improved possibilities for reporting and follow-up on regulatory activities and approval status