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Federal Regulations and Guidelines

OHRP - Office for Human Research Protections, DHHS
45 CFR 46 - DHHS regulations for the protection of human subjects
45 CFR Parts 160, 162 and 164 - Health Insurance Reform: Security Standards; Final Rule
Exempt Guidelines - Categories of research that may be reviewed by the IRB through an exempt review procedure
Expedited Guidelines - Categories of research that may be reviewed by the IRB through an expedited review procedure

OHRP - Office for Human Research Protections, DHHS
45 CFR 46 - DHHS regulations for the protection of human subjects
45 CFR Parts 160, 162, and 164 - Health Insurance Reform: Security Standards; Final Rule
Exempt Guidelines - Categories of research that may be reviewed by the IRB through an exempt review procedure
Expedited Guidelines - Categories of research that may be reviewed by the IRB through an expedited review procedure

Good Clinical Practice: Consolidated Guidance - guidance for investigators, sponsors, and IRBs
Good Clinical Practice in FDA-Regulated Clinical Trials - FDA website for investigators conducting clinical trials

Belmont Report - Ethical principles and guidelines for the protection of human subjects of research
Declaration of Helsinki - Recommendations guiding medical doctors in biomedical research involving human subjects
Nuremberg Code - Directives for human experimentation

Contact Us

IRB Email: elpasoirb@ttep.edu
IRB Physical Address: 137 Rick Francis St., MSBII
IRB Mailing Address: 130 Rick Francis St., MSB II
El Paso, TX 79905