Simplify the process of managing, validating and exchanging ‘trusted’ product master data and achieve regulatory compliance, reduce procurement spend and ensure patient safety.
Simple. Scalable. Global.
100% Certified. Globally Proven.
GAMP 5 validated and 21 CFR Part 11 compliant for UDI submission to FDA.
Product Information Management
Create a centralized management process for managing products, images & attachments.