Sponsor / CRO

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

Please view the links below to obtain information on investigator responsibilities, IntegReview reporting requirements, investigator training, and other useful links regarding federal regulations and guidance on conducting research.

Sponsor/CRO Responsibilities
IntegReview Reporting Requirements
Training Links
Regulation and Guidance Documents
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Sponsors may obtain answers to questions, express concerns, and convey suggestions regarding IntegReview’s Human Research Protection Program (HRPP) via e-mail to Betty Olivarez, Director of Compliance or by dialing (512) 326-3001, extension 211.

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