Streamline study operations, manage data securely, and keep on top of compliance, all using Knack’s no-code platform.
Participant Registry
Knack lets you scale trial apps as your needs evolve without expensive IT builds. Launch a system quickly, customize as processes change, and get built-in support when you need it.
A no-code clinical trial management system allows research teams to build and manage study workflows, such as participant tracking, data collection, and reporting, without needing developer skills.
Knack centralizes all aspects of your trial, from participant data to protocols, documents, and reporting, into one secure platform. This eliminates manual tracking, reduces errors, and improves coordination across research teams and study sites.
Yes, Knack is designed to support multi-site coordination by providing real-time access to shared data, standardized workflows, and role-based permissions. This ensures all stakeholders stay aligned, regardless of location.
Knack offers HIPAA-compliant infrastructure, encrypted data storage, and detailed audit logs to support regulatory requirements such as FDA 21 CFR Part 11 and IRB oversight. This helps ensure your study data remains secure and audit-ready.
You can build a wide range of workflows, including participant registries, protocol tracking systems, study dashboards, document repositories, and audit logs. Each system is fully customizable to match your specific study design and operational needs.
Most teams can build and launch a functional clinical trial management system in a matter of days or weeks, depending on complexity. Because no coding is required, you can iterate quickly and adapt your system as your study evolves.
