ClinicalTrials.gov Requirements | Human Subjects Office
https://hso.research.uiowa.edu/clinicaltrialsgov
RegistrationA. Who Is Required to Register?B. When Must I Register on ClinicalTrials.gov?C. What Should I Do After Registration?D. Getting Started - ClinicalTrials.gov ChecklistApplicable Clinical TrialsNIH and ICMJE Reporting RequirementsResults Submission and Required DocumentsObservational and Expanded Access StudiesProtocol Registration and Results System The Protocol Registration and Results System (PRS) is the database where information published on ClinicalTrials.gov is entered. To access the PRS, investigators should go to register.clinicaltrials.gov. The PRS consists of two sections: the Protocol Section and the Results Section. The Protocol section is where registration information is entered ...
The Protocol Registration and Results System (PRS) is the database where information published on ClinicalTrials.gov is entered. To access the PRS, investigators should go to register.clinicaltrials.gov. The PRS consists of two sections: the Protocol Section and the Results Section. The Protocol section is where registration information is entered ...
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