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Clinical Trial Execution

  • Site selection and feasibility assessments
  • Regulatory submissions
  • Investigational product management
  • Study monitoring
  • site management
  • Patient recruitment
  • Data collection
  • Quality assurance
  • Timeline planning and management
  • Budgeting and resource allocation
  • Risk assessment and mitigation
  • GCP compliance
  • Audit preparation and support
  • SOP development and training
  • Supply chain management
  • Central laboratory services
  • Vendor management and oversight