SITE MANAGEMENT

D2L has emerged as one of the best Site Management Organisations for clinical projects of pharmaceutical, biotech, medical device and healthcare organizations. With many years of experience in conducting Phase II– IV clinical trials and recruiting and managing thousands of patients at multiple sites, D2L exhibits immense confidence and competence to manage smaller to large scale Clinical trials. We provide following expertise services to our Clients’:

  • Site Feasibility & Planning
  • Clinical Site Preparation & Upgradation
  • Trial Agreement Assistance
  • Site Training & Staffing of CRCs
  • Essential Documents Management
  • Electronic Data Capture (EDC) Support at Sites
  • Ethics Committee (EC) Submission
  • Regulatory clearances Support
  • Patients Recruitment Coordination
  • Patients follow-up & Study compliance
  • Data compilation & query resolutions
  • Site Inventory Management
  • Study Monitoring & Site close-out operations
  • Centralized Project Management
  • Site & Investigator Payments Management
  • Project Compliance Monitoring & Audit
  • Quality Assurance including Training