Overview

ICTU Global has capabilities and proven experience in providing clinical trial delivery including: 

• Conception/design of trial
• Ethics applications and submissions
• Sites selection and set-up.  This includes contract and financial negotiations  
• Sites initiation visits/training – this covers study objectives and e-CRF training
• Recording and maintaining study’s essential documentations and trial master files

 

• Overseeing site’s investigator’s site files
• Monitoring sites’ recruitment progress ensuring the performance is on par with study milestones
• Point of contact for any sites’ recruitment, data queries
• Overseeing study’s finances – i.e. payment of sites’ set up fees, recruitment fees 
• Study close-out activities