Study Design
  Study Feasibility Assessment
  Clinical Development Plans


  Phase II to IV Studies
  Collaboration with Medical Faculties
  Drug Development programs
  Patient Registries
  Biometric Identification of Patients


  Collections from different centres
  Traceability of Results
  Networking of Analyzers


  Study Initiation
;   Patient Recruitment and Retention
  Clinical Monitoring
  Project Management

  CRF Design
  Database Design
  Document Management
  Data Capture


  Biostatistical Consultancy
  Statistical Analysis and Reporting
  Training on SAS (Version 8.2)


  Medical Monitoring
  Protocol Development
  Pharmacovigilance