SciNote helps you manage your laboratory (R&D) processes in compliance with GxP and Title 21 CFR Part 11 regulation.
The software itself cannot be 'compliant', but SciNote has features that allow you to set up, manage and record your processes in compliance with the cited regulatory standards. These types of standards typically require lots of traceability that SciNote offers. However, it is important to understand 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 feature in your SciNote account (21 CFR Part 11 add-on) please fill out this form.