Creating a clinicaltrials.gov Record When you are entering your study into clinicaltrials.gov (CT.gov) please be aware of a few things. 1 Confirm that the study needs to be registered. COMIRB determines FDAAA applicabili - Clinical study design - Document - PDFSEARCH.IO

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	Creating a clinicaltrials.gov Record When you are entering your study into clinicaltrials.gov (CT.gov) please be aware of a few things. 1 Confirm that the study needs to be registered. COMIRB determines FDAAA applicabili Add to Reading List Document Date: 2014-12-01 13:50:56 Open Document File Size: 251,97 KB Share Result on Facebook City Room N3214 / Unique Protocol / / Company BP / CBC / Colorado Multiple Institutional Review / / / Event Person Communication and Meetings / / Facility University of Colorado Denver Responsible Party / University of Colorado / / IndustryTerm biologic products / / MedicalTreatment liver transplant / / Organization University of Colorado / FDA / National Institute of Health / Clinical Research Support Center / Data Monitoring Committee / Colorado Denver Responsible Party / University of Colorado Denver COMIRB / / / Position Governor / general public The / general public audience / coordinator / RePORTER / Sponsor-Investigator / / Product testosterone / / ProvinceOrState Aurora / Colorado / / URL http / SocialTag Medicine Clinical research Food and Drug Administration Design of experiments Drug safety Clinical trial ClinicalTrials.gov Institutional review board Investigational New Drug Research

Creating a clinicaltrials.gov Record When you are entering your study into clinicaltrials.gov (CT.gov) please be aware of a few things. 1 Confirm that the study needs to be registered. COMIRB determines FDAAA applicabiliAdd to Reading List