Allyfe

Allyfe offers a smart, modular document management platform designed for Sponsors, CROs, and Clinical Sites. Our flexible system spans Site Start-Up (SSU), digital Investigator Site File (ISF), and electronic Trial Master File (eTMF), including a compliant archiving solution. This modularity allows clients to use Allyfe as a standalone system or integrate it seamlessly into existing workflows—supporting both clinical trial execution and long-term archiving needs. All modules adhere to strict security and regulatory standards and are fully aligned with the DIA TMF Reference Model. Allyfe ensures high-quality, compliant document management with real-time monitoring and built-in quality control—all within an intuitive, user-friendly interface.