Drug

  • Phase I-III Clinical Trials
  • Phase IV, Patient Registry
  • Protocol Development and Study Design
  • Project Management
  • Clinical Trial Monitoring
  • Trial Master File Management and Online Archival
  • Statistical Consultation and Analyses
  • CRF Development (Paper or eCRF)
  • Data Management
  • Medical (Event and Medication) Coding
  • Quality Assurance Audits (Vendor, Process, and Database Audits)
  • DSMB/DMC/SRC Charter/Meeting Coordination
 
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