Applying Ethics and Integrity to Human Research
IntegReview reviews the following types of research: Phase I-IV drug/biomedical, medical device, social and behavioral, Investigator-sponsored, single and multiple investigator as well as research conducted in academic and hospital settings, expedited review for research that qualifies, expedited review of additional Investigators, research determined to be exempt, research conducted in Latin America and Canada.
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IntegReview Ethical Review Board
3001 S. Lamar Blvd., Suite 210
Austin, TX 78704
Phone: 512-326-3001
Fax: 512-697-0085
Email:

Sponsor/Project Manager

In an effort to enhance IntegReview’s Human Research Protection Program (HRPP), we would like to provide sponsors and Project Managers of clinical research with information on their responsibilities, and reporting requirements.

The links below are provided to offer this information and to also provide information on training/educational conferences, as well as other links we feel will be helpful regarding federal regulations, guidance on conducting research, etc.

Sponsors may obtain answers to questions, express concerns, and convey suggestions regarding IntegReview’s Human Research Protection Program (HRPP) via e-mail to Robert Orozco, Director of Compliance or by dialing (512) 326-3001, extension 207.

Please feel free to complete IntegReview’s Customer Survey if you have any suggestions to offer or if you would like to voice any concerns regarding our processes or services.