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Resources to help you navigate the IRB process.

  • What IRB Regulations Apply When? When HHS Regs (45 CFR 46) Apply vs. FDA Regs (21 CFR 50 and 56)

    An overview of the two sets of IRB regulations that might apply to your research and their similarities/differences.

    8/15/2025

  • Unified IRB Submission Checklist for Startups: Key Components and Approval Criteria for Human Subjects Research

    A comprehensive checklist to ensure your IRB submissions are complete and meet regulatory requirements.

    8/10/2025

  • When Do You Need IRB Approval? Legal vs. Practical Requirements for Human Subjects Research

    The legal and practical differences on when IRB approval is needed for startups.

    8/5/2025

Tempus IRB

OHRP registration numbers:

IRB00014644

IORG0012374

Tempus IRB is governed by, and adherent to, 45 CFR 46, 21 CFR Parts 50 and 56, HIPAA (where applicable), and other relevant regulatory frameworks.

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