Topics Map > OnCore > Data Field Definitions > Oncology
Topics Map > OnCore > Data Field Definitions > Non-oncology

Sponsor Type

Field Name Definition Requirement
Entry Instructions		 Responsible for Entry QA
Sponsor Type Industry: Design and implementation of the study is controlled by the pharmaceutical company. If two pharmaceutical companies are involved, check the one as “principal” that is ultimately responsible for reviewing the data and study conduct oversight.
Institutional: In-house clinical research studies authored or co-authored by UW investigators. The UW investigator has primary responsibility for conceptualizing, designing and implementing the clinical research study and reporting results.
It is acceptable for industry and other entities to provide support (e.g., drug, device, other funding) but the trial should clearly be the intellectual product of the center investigator.
This category may also include:
  • Institutional studies authored and implemented by investigators at another Center
  • Multi-Institutional studies authored and implemented by investigators at your Center
  • External Peer Reviewed Studies: R01s, SPORES, U01s, U10s, P01s, CTEP, or any other clinical research study mechanism supported by the NIH or an approved peer-reviewed funding organization.
 Required OnCore support staff No

Keywords:
Sponsor Type 
Doc ID:
101795
Owned by:
Molly H. in SMPH Research Informatics
Created:
2020-05-07
Updated:
2022-11-29
Sites:
SMPH Research Informatics