« SciNote Blog

Compliance

Compliance with FDA 21 CFR Part 11 Key Things to Know blog

Historically, companies maintained a paper trail of all their equipment, experiments and results in order to comply with cGMP (Current Good Manufacturing Practices) and cGLP (Current Good Laboratory Practices) regulations.

From defining your needs, to narrowing down the selection, testing an electronic lab notebook (ELN) and presenting it to your team, this electronic lab notebook guide will provide valuable tips on how to approach the process.

E-signing Tasks in SciNote blog

Together with the new Task status flow, we also made some improvements for e-signing Tasks in SciNote. Do not worry, the basic principles for e-signatures are still the same and still comply with the GxP and 21 CFR Part 11 requirements.

Connecting inventory items to your tasks blog

To address the need of connecting the information about samples, reagents, instruments, or other inventory items, to your work on experiments and tasks in the lab, we are adding new functionalities to SciNote. 

Identify re-usable modules in your workflows (and use them as templates) blog

When working with simple to-do lists or simple protocols, documenting and executing them is straightforward: all to-dos or protocol steps are listed in a single checklist or in one protocol.

Exporting All Your Data in A Readable Format from SciNote blog

SciNote Premium Academia and Industry accounts now enable you to export all your projects’ data in a readable format. And it gets even better – all your attachments will also be neatly organized in folders.