Easily manage the entire lifecycle of IRB protocols
Your organization’s integrity depends on ensuring research is ethical. But that can be difficult when protocol processes are lengthy and convoluted. And if your systems are manual or outdated, that limits visibility into protocol status even more.
Get transparency into all phases of a protocol with Human Ethics. Enjoy increased efficiency with 100% electronic preparation, submission, and routing of human research study protocols. It’s never been easier for administrators, researchers, and committee members to collaborate.
Faster, more compliant human protocol management
Human Ethics integrates with your existing systems, and reporting CITI® training is easy
Accelerate review process
Improve transparency and collaboration
Reduce noncompliance risk
Smart forms for faster protocol development
Make researchers happy by saving them valuable time developing protocols with configurable smart forms:
- Familiar form templates developed with an AAHRPP-accredited partner
- Intuitive drag-and-drop builder
- Ability to revert to previous drafts
- Skip logic or conditional branching allowing for answering questions relevant to the study
Collaborate online for submission, review, and approval with electronic routing, system alerts, and notifications
Compare submissions side by side for faster protocol review
See activity pipeline and protocol status with role-based dashboards and automatic reminders
Manage meetings with increased efficiency and compliance
Improve collaboration among administrators, researchers, and committee members with electronic protocol preparation, submission, and routing.
Increase transparency of animal research protocols. Shorten turnaround time for protocol review and approval while reducing noncompliance risks.
Stay compliant, reduce approval time, and remove complexity from the protocol process. Keep research on schedule with improved collaboration and transparency.
Make the disclosure process painless and increase faculty participation. Complete, track, and manage disclosures in minutes for more efficient research administration.
Expedite the protocol approval process and foster a culture of safety by automatically cross-referencing staff qualifications with research activities.
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