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What It's About

This white paper explores microscopy and GxP compliance with Labtwin, demonstrating how researchers can safely annotate microscopic findings (such as drug efficiency and toxicity) in low-light conditions while ensuring seamless transitions from R&D to commercialization in regulated industries.

 

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Who it’s for

This is made for, scientists & researchers working in microscopy, pharmaceutical & biotech professionals managing drug development, and regulated industry teams needing compliant digital documentation.

Who is the white paper for?
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How to use it

Labtwin’s user-based Audit Trails ensure real-time, compliant documentation without pen and paper, allowing for uninterrupted, regulation-ready experiments. Download the white paper to learn how Labtwin’s digital lab assistant can streamline documentation and compliance.

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Frequently Asked Questions

Is this really free?
Absolutely! We're sharing this free knowledge that we hope you'll find useful. Keep us in mind next time you have LIMS questions.
Why do I need to share my information?
We ask for your personal information so we can provide you with important details about the white paper, including access links and any follow-up materials. Your information also helps us tailor future content to your needs. Rest assured, your privacy is important to us, and we will never share your information without your consent.
Who wrote this white paper?
Our white papers are always written in-house with the assistance of our expert consultants.