 |
|
 |
 |
 |
|
|
| |

Clinical Trials
In order for a study to be considered a "Clinical Trial", the study must involve ALL of the following elements:
- Intervention (either biomedical or behavioral)
- Human Interaction (beyond the informed consent process)
- Outcome Variables (measures safety and effectiveness of intervention)
- Prospective Design (Phases I, II, III, IV)
These are processed by the Office of Clinical Trials Administration (OCTA) within the Institute for Clinical Research (ICR), which can be reached in the following ways:
Mail: 1300 York, Box 305
Office: Room A-131
Phone: (212) 746-3774
E-mail: OCTA@med.cornell.edu
Web site: ICR
|
 |
|
Contact

Grants and Contracts
Mail: 1300 York, Box 89
Location: 425 E. 61st, Rm. 223
Phone: (212) 821-0959
Email: rasp@med.cornell.edu
|
|