Our Services

Our Services

I. Phase II to Phase IV Clinical Research
  • PRE-TRIAL
    1. Identify sites and PIs
    2. Regulatory and IRB submission & approval
    3. Site set up
    4. Prepare and maintain clinical research documentation
  • DURING THE TRIAL
    1. Assist in recruitment of subjects
    2. Coordinate subject related activities but not limited to dosing & follow up visit procedures
    3. Coordinate Monitoring & Audit visits
    4. Prepare and maintain trial specific files
    5. Focus on safety management of subjects
  • POST-TRIAL
    1. Coordinate close out visit including financial reconciliation of trial
    2. Resolve data queries
    3. Archival of study documents
II. Post Marketing Surveillance Studies
  • Data Management and Biostatistics
    1. Data entry and validation
    2. Statistical assessment report
III. Medical Writing Services
  • All essential documents of clinical research
  • Manuscript writing for publications