Human Subject Research Portal Children's Hospital Colorado
A new, online "one stop shop" site where researchers, study coordinators and others involved in human subject research can easily navigate the project approval process. This single entry portal will eliminate redundancy and avoid confusion for those engaged in Human Subject Research. What is it? www.UCDenver.edu/HSRPortal
Portal Overview
Which institutions will use the portal? Piloting the process University of Colorado Hospital Children’s Hospital Colorado UCDenver Clinical and Translational Research Center (CTRC) Existing Process Veteran’s Administration Denver Health National Jewish (non CTRC) Boulder (non CTRC)
Which protocols will use the portal? University of Colorado Hospital All Submissions: Industry, federally funded and internally funded, (including Expedited, Exempt, Non Human Subject Research) Children’s Colorado Federally funded, Investigator-Initiated, Industry Funded (Full Board only) UCD Only Federally funded or Investigator-Initiated (Full Board) CTRC All protocols requesting use of CTRC resources Aim is to eventually have all studies using the portal at this point each institution is piloting If you are unsure follow submission instructions which will assist in making this determination.
Which protocols will require Scientific Review? Investigator-Initiated, Internally funded Some foundation funded studies (if not peer-reviewed as part of the funding process) Federally reviewed grants (including training grants) where the science has significantly changed since the grant was peer-review
Which protocols will not require Scientific Review? Industry Funded (protocol funded and owned by industry) Multisite Studies (where UCD is not the lead site) Those that receive FDA review as part of an IND or IDE clearance Federally funded grants (not including training grants) where the science has not significantly changed since the review
Advantages Facilitates parallel submission Single feedback letter which avoids conflicting requests for changes Tracks submission timelines and deadlines Reduces the complexity of navigating the current protocol approval process Advantages