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.
- Sponsor/Project Manager Responsibilities
- IntegReview Reporting Requirements
- Training Links
- Regulation and Guidance Documents
- Adobe Acrobat Reader
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.