Use of JDE E1 in Medical Device manufacturing environment.

David Zepp

I hope this is the best forum for this general request....

I'd like to connect with others who are using JDE E1 in a Medical Device manufacturing environment. I'm new to JDE E1 and would like to understand to what degree others have addressed regulatory requirements (ISO 13485, FDA parts 820, 211, 11) within the JDE software either through a native module or through third party software integration. Ultimately I'm looking for a high degree of ERP/Quality System integration, and I'd like to understand how well others have been able to integrate.

Please let me know if you would be open to discuss, or if I should be posting elsewhere.