Clinical Trial And Project Management

QUADRO CRO performs and handles project management for Clinical Trials, Observational Trials, and Compassionate Use Programs according to ICH GCP and applicable regulatory requirements.

We provide the following services for local or international studies:

• Site Feasibility and Selection
• Site Initiation
• Site Monitoring
• Site Close-out
• Inventory Keeping of Trial Supplies
• Planning and Coordination of Investigator Meetings
• Importation and Customs Procedures
• Trial-specific Training
• Site-specific Dossier Management
• SAE Surveillance and Collection
• Contract Negotiations with Laboratories
• Contract Negotiations with Rotating Fund Directorates.