We are a small company looking for a solution that meets Part 11 security requirements. Has anyone accomplished this? I know a lot of pharmaceutical companies have done this. I am strong user and intermediate administrator but I have not been involved with setting it up (and documenting) in a way to meet these requirements. To start, do we need to purchase the Premium version or will the Standard version suffice? What add-ons are you using? How are you documenting that JIRA is compliant with the regulations.
Hi @Jim Test Account -- I realize this post is a few months old already...is this still something you're exploring? I have a lot of experience configuring Jira for Part-11 compliance, and so I might be able to help you out.
Some quick answers:
You need to consider a lot of stuff when complying with Part 11 in Jira. In most cases, you'll have to combine built-in functionality with some plugins from the Marketplace. Jira offers an audit log for some system changes:
For changes within the issues list made by users (including deleted ones) and export, you can try the Issue History plugin. It's developed by my team.
Additionally, you'll need the e-signature fields plugin.
Also, this article can be helpful:
Jira for CFR 21 Part 11 compliance: how to get audit trail for FDA inspection
You must be a registered user to add a comment. If you've already registered, sign in. Otherwise, register and sign in.
Online forums and learning are now in one easy-to-use experience.
By continuing, you accept the updated Community Terms of Use and acknowledge the Privacy Policy. Your public name, photo, and achievements may be publicly visible and available in search engines.
You must be a registered user to add a comment. If you've already registered, sign in. Otherwise, register and sign in.