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.
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.

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.
