Tag: Manufacturing Supply Chain

Presented by: OASIS Medical, Inc SmarterCommerce by Premier  Session ID 109160, Presented at COLLABORATE17After selecting JD Edwards EnterpriseOne to support its operations and beginning 9.1 impleme

All FDA regulated industries must produce either a “Batch Record” or a “Device History Record” that documents all the activities that went into the manufacture of a given product lot, batch, or device.  An electronic approach is highly desirable and now is possible using the electronic records and signatures captured through EnterpriseOne’s Data Change Tracker application built into the JDE Toolset.

All FDA regulated industries must produce either a “Batch Record” or a “Device History Record” that documents all the activities that went into the manufacture of a given product lot, batch, or device.  An electronic approach is highly desirable and now is possible using the electronic records and signatures captured through EnterpriseOne’s Data Change Tracker application built into the JDE Toolset.