Submitting a Clinical Trial

Complete Block Study Block IND and IDE Submissions Additional Block IRB Block Budge Block Subject Block EMR Block Investigational Block Clinical Research Regulatory Maintenance
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laws     it-tech-apps             
    learn-about. learn-about-device  clinical-engineering  reviewirbsop reviewctsc     open  overview-drug-mgmnt

 

 

read-ct-sops   preclinical device  radiation-committee prepare   complete  informed-consent  enter distribution.  report-new-info  report-new-info
citi-training   determine investigationaldeviceexemp  bio-use-authorize  submit-initial  prepare-internal-budget  pps  research-study-maintenance  prescribing

 

 report-serious
umn-mandatory-training   investigationaldrugapp abbreviated stem-cell-research-oversight   respond-to-irb  negotiate submit-copy-consent   associate  ids-charges report-protocol-deviations  report-protocol-deviations
umn-privacy-security-training   expanded emergency  scientific-review  fileapprovals    payments   dietarysupplements2  submit-continuing submit-cder 
    newdrugapp pma      ct-contracts  drawing  associate-orders  compounding  maintain-study
    dietarysupplements humanitarian        clia-waved  billing-review     study-monitoring
    learn-about-sponsors        subject        
    createdsmb                
                     
epic-emr-billing   postinfo                
coi-training