Cytodyme helps biotech teams move faster through clinical development by simplifying cGxP documentation.

Automate new document creation. Build and revise clinical documents of all kinds using powerful AI workflows—supporting SOPs, material specifications, batch records, IRB submissions, and more—while enabling teamwork, collaboration, traceability, and speed across your entire development process.

Get submission-ready faster with smart guidance, automated report generation, and built-in compliance checks. Reduce errors with automated cross-checking and contextual prompts that help complete each step with clarity and confidence.

AI supports the process, but never trains on your data. Your IP stays protected with enterprise-grade security.

Book a demo to see how Cytodyme keeps your team focused on the science—not the paperwork.