Services

Services

We provide a full range of activities required for the regular and legal conduct of a clinical trial. These include:

  • Site selection, feasibility and evaluation
  • Negotiation of contracts with institutions and investigators
  • Regulatory submissions and obtaining of approvals
  • Obtaining import permits and organizing the import of study medication and all study materials
  • All monitoring activities including Site Initiation Visit, interim Monitoring Visits and Close-Out Visits
  • SUSAR reporting; drug safety reporting
  • 24 hour expert support
  • Communication between trial sponsor and trial site
  • Monitoring (phases I-IV)
  • Pharmacovigilance
  • Translation of clinical trial-related documentation
  • Specialized medical and certified translations