UR Medicine Clinical Trials Office
GPTKB entity
Properties (55)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
legal case
|
| gptkbp:collaboratesWith |
researchers
|
| gptkbp:conducts |
feasibility studies
patient recruitment strategies clinical trial audits site initiation visits |
| gptkbp:coordinates |
study logistics
|
| gptkbp:engagesIn |
community outreach
protocol amendments quality assurance activities |
| gptkbp:ensures |
compliance with regulations
ethical conduct of research |
| gptkbp:facilitates |
investigator-initiated trials
patient follow-up research partnerships data monitoring committees investigator training |
| gptkbp:focusesOn |
clinical research
|
| https://www.w3.org/2000/01/rdf-schema#label |
UR Medicine Clinical Trials Office
|
| gptkbp:maintains |
clinical trial registries
|
| gptkbp:manages |
clinical trial data
investigator budgets |
| gptkbp:offers |
consultation services
regulatory guidance data management services patient recruitment services research training programs protocol development assistance research compliance training clinical trial insurance guidance |
| gptkbp:participatesIn |
multicenter trials
|
| gptkbp:partOf |
gptkb:UR_Medicine
|
| gptkbp:promotes |
patient safety
|
| gptkbp:provides |
educational resources
data analysis services monitoring services clinical trial resources support for clinical trials patient consent processes statistical support site selection services clinical trial management software adverse event reporting services clinical trial feasibility assessments |
| gptkbp:supports |
patient education
regulatory submissions collaborative research initiatives clinical trial innovation clinical trial funding clinical trial publications |
| gptkbp:utilizes |
electronic data capture systems
|
| gptkbp:worksWith |
pharmaceutical companies
sponsors institutional review boards clinical research organizations |