Our Services
Fast, objective, and transparent IRB reviews for all types of human subjects research.
Overview
Timely IRB handles all types of human subjects research, from minimal risk studies to complex clinical trials. Our services are designed to accelerate the launch of your research while ensuring compliance to the OHRP and/or FDA standards for human subject protection.
The Timely Difference
Timely IRB
- Review & decision in hours
- Flat-fee pricing
- Transparent review process
- Easy, streamlined submission
Traditional IRBs
- ✗Weeks or months for review
- ✗Complex, unpredictable pricing
- ✗Opaque decision-making
- ✗Burdensome submission process
Process Timeline
Submit Your Study
Use our streamlined online submission system to provide your study details.
Initial Review
Our expert reviewers begin the assessment within minutes of submission.
Feedback (if needed)
Receive clear, actionable feedback within hours if any changes are required.
Approval
Receive your approval within 12 business hours of submission.
Timely IRB's clear and transparent review process ensures your research moves forward quickly, objectively, and without surprises. Learn more.