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.

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 and guidance on conducting research, etc.

Sponsor/CRO 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 Melanie Flores, Vice President of Compliance or by dialing (512) 326-3001, extension 209.