What We Do

What can we do for you?

Based on your specific needs we can offer you customized solutions in:

  1. Feasibility studies
  2. Audits
    • Vendor qualification incl CRO audits
    • Site audits
    • Pre-Inspection audits
    • Trial master file and other document review
  3. Monitoring
    • Bioequivalence studies
    • PK studies in patients
    • Early phase studies
  4. Medical Monitoring
  5. Pharmaco-vigilance support in PSUR & CIOMS development
  6. Customized Training Programs
    • GCP
    • Quality Systems
    • PI Training
  7. Medical Writing and review
    • Protocol writing & review
    • CRF design & review
    • Clinical study report
    • Investigator Brochure
    • Product updates & brochures
    • SOPs Development & review