Our Services

Fast, objective, and transparent IRB reviews for all types of human subjects research.

Overview

Tempus 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 Tempus Difference

TempusIRB

  • 12-hour review guarantee
  • 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

1

Submit Your Study

Use our streamlined online submission system to provide your study details.

2

Initial Review

Our expert reviewers begin the assessment within minutes of submission.

3

Feedback (if needed)

Receive clear, actionable feedback within hours if any changes are required.

4

Approval

Receive your approval within 12 business hours of submission.

Tempus IRB's clear and transparent review process ensures your research moves forward quickly, objectively, and without surprises. Learn more.