SciNote helps you manage your laboratory (R&D) processes in compliance with GxP and Title 21 CFR Part 11 regulation.
SciNote features allow you to set up, manage and record your processes in compliance with the cited regulatory standards.
However, it is important to understand that it is still up to the organization to comply with the regulatory requirements - no software can do that on behalf of the organization.
If you require electronic signatures and audit trail features, check out SciNote Premium Industry Plan that comes with the 21 CFR Part 11 add-on. If you need more information, please fill out this form.