The QuickSTART program is designed to help clinical trials sites and industry sponsors establish standardized processes to improve efficiency and achieve a 90-day overall start-up time for clinical trials – months faster than the current standard.
QuickSTART is a streamlined start-up process supported by CTO and an online digital platform in which engaged parties (sponsor, investigator and institution) agree to work in a streamlined fashion toward a 90-day study start-up goal. The clock starts ticking when sponsors send final study documents to their selected sites. Within 90 days, QuickSTART helps make sites activated and enrollment ready.
A QuickSTART Ready industry sponsor selects a new study opportunity.
Sponsor identifies a QuickSTART Ready site that is feasible for the study.
Sponsor, site and investigator agree to using the QuickSTART approach.
Sponsor creates an application on the QuickSTART digital platform and submits to the site with full study document package. 90-Day countdown begins!
Sites and sponsors use interactive QuickSTART portal to complete contracts, budget and approvals within 90 days.
QuickSTART Ready sites have registered as users on the QuickSTART platform and have committed to using a streamlined start-up approach within a target of 90 days. If you would like to become QuickSTART Ready, please contact us for more information.
|Hamilton Health Sciences
|Northeast Cancer Centre of Health Sciences North
|North York General Hospital
|The Ottawa Hospital/OHRI
|Southlake Regional Hospital
|Lawson Health Research Institute (London Health Sciences Centre / St. Joseph’s Health Care London)
|University Health Network
Information for QuickSTART Ready institutions.
Introduction to the QuickSTART digital platform.
A customizable budget building tool.