Create and manage IRB protocols with dynamic forms, pre-populated data, and real-time approval status visibility.
Make the submission process smoother and faster, reducing errors and eliminating bottlenecks that slow down approval timelines.
Speed up the approval process by automating routing and notifications, ensuring your protocols get reviewed and approved quickly without unnecessary delays.
Easily navigate the strict regulatory requirements with built-in guidance, helping investigators and coordinators stay on track and ensuring full compliance at every step.
It’s much easier. The IRB module offers smart forms that streamlines the compliance process and can be adjusted as per your requirements. It allows you to reference relevant details from other systems, such as IACUC and IBC, eliminating the need for repetitive manual entry. Plus, it flags potential compliance issues early, helping you stay on track and save time.
Yes, the IRB module integrates smoothly with the systems you already rely on. Whether it’s your clinical trial management system (CTMS), electronic health records (EHR), laboratory management systems (LIMS), or document management platforms like SharePoint or cloud storage solutions, everything connects effortlessly. This smooth integration capability of our IRB module enables data flow across departments, reducing the need for manual data entry, minimizing errors, and providing real-time, accurate information to support faster, more efficient decision-making.
The module provides real-time alerts for any potential compliance issues, ensuring all submissions and amendments meet regulatory standards before they are submitted. AI-driven workflows guide users through every step, flagging any discrepancies early in the process.
Yes, the module tracks protocol amendments and renewals by keeping a centralized record of all changes, ensuring compliance with ongoing research requirements and preventing missed deadlines.
The IRB module helps speed up the approval process by verifying that all required components of the protocol submission have been completed before submission, ensuring all relevant details are in place. It keeps things moving with real-time notifications and document tracking, reducing the time spent waiting for approvals and making the whole process more transparent.
The IRB module takes care of protocol versioning automatically. Every time there’s an amendment or update, the system keeps track and ensures that only the latest version is being used. This way, you’re always working with the right, compliant version, without worrying about missing or outdated information.
The IRB module uses top-tier security protocols, including data encryption, secure cloud storage, and role-based access controls, to ensure that sensitive research data remains protected throughout the submission and review process.
