Experience how a modern, cloud-based eQMS can streamline compliance and simplify quality processes – without the commitment. Following a brief introduction call, qualified teams will receive access to a fully functional trial environment tailored to life sciences and other highly regulated industries.
What to Expect:
Access to core modules: Document Control, CAPA, Training, Audits, and more
Pre-configured demo aligned with FDA, GxP, ISO, and MDR compliance needs
Explore user-friendly, no-code workflows on the trusted Now Platform
Gain insights with real-time dashboards and audit-ready reporting
Start the process with a quick intro call to qualify for your trial.