I have just been asked about FDA CFR Part 11 compliance (IVD - in vitro diagnostics) with respect to JIRA. After a quick search I found some plugins that add e-signatures but what I would really like to know is, are there any whitepapers or the like, about using JIRA in a way that meets these regualtions? Whats involved etc..
If there are any users out there who are FDA compliant and using JIRA it would be grteat if perhaps you could message me. I am just after afew pointers on whats involved etc.
Hi Nick -
I think same Nick that called us yesterday? Not sure..
This was created for FDA Compliance - however, FDA specifications are vast and I think there is alot of interpretations to what "compliance" means.
AppFusions does not purport to be FDA audit cops - only a solution provider to meet an audit requirement. We provide a solution, which you can trial and evaluate - and determine if it meets YOUR interpretation of FDA compliance. These bars/requirement needs may vary, depending on the type of supplier you are.
I will confirm that the plugin was created for exactly FDA compliance purpose, and not by our interpretation of what FDA compliance meant, but by a medical instrument corporation. It is also being used by other corps that evaluated it and felt it met their FDA Compliance audit needs.
It also can be extended, upon request. I expect it also will evolve in time.
Hope this helps.
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