A clinical trial can be a complicated and lengthy ordeal. At Q-Trials we take care of all aspects for you and make it seem easy. However, if you are a newcomer to this world, you might benefit from understanding the scope of what we do. Here is a simplified scheme which includes all major milestones of a classic clinical trial.

1. Q-TRIALS
TRIAL SIMULATION

2. Trial Simulation
Close–Out
Follow-Up
Treatment
Patient Recruitment
Study Initiation
Primary Submissions
Feasibility & Site Selection

3. Feasibility & Site Selection
 Using our connections with leading
investigators
 Estimating recruitment and treatment
potential

4. Primary Submissions
 Preparing submission packages
 Correspondence with MoH and local
committees until approvals are granted
 Translations
 Import of investigational product and lab kits

5. Study Initiation
 Initiating all sites
 Investigational product and lab kits distribution

6. Patient Recruitment
 Monitoring recruitment and consent process
 Coordinating collections of biological samples
for a central laboratory
 Ensuring achievement of recruitment goals

7. Treatment
 Monitoring
 Coordinating collections of biological samples for
a central laboratory
 Monitoring pharmacy, patient
randomization, prescriptions
 Ensuring site compliance or reporting deviations
 Ensuring achievement of treatment goals
 Interim submissions and reports
 Import and distribution of investigational product
and lab kits, return to depot and destruction
 Translations

8. Follow-Up until Close–Out
 Follow-Up
 Monitoring – patient FU process and site
adhering to timelines
 Ensuring closure of all queries and pending
issues
 Closing pharmacy and investigational product
return to depot
 Closing site and collecting all data
 Close-out submissions