Data Sheet
MasterControl eMDR Enhanced Forms
Loading Content
About this Document
MasterControl eMDR enables you to digitize your adverse event reporting process and integrate it with your quality management system. The best practice solution is designed to meet the requirements for digital forms processes within FDA-regulated and GxP environments, including compliance with 21 CFR Part 11. This data sheet provides an overview of the features and benefits of the solution.
PDF
— 0.08MB
