Clinical Trials (phase II – IV)

Therapeutic Equivalence (non-Inferiority) Studies

for Locally Applied/Acting generic products (Ophthalmic, Dermatological, Intra-Vaginal, Inhalers)

Superiority Studies

for Fixed-dose Combination Products

Investigator Sponsored Studies

Observational Studies

  • Study design, protocol, e-CRF & ICF development
  • Study conduct
    • Clinical site selection, recruitment, initiation, monitoring, close-out
  • Study site management
  • Data management
  • Statistical analysis
  • Clinical Study Report
  • Investigator & study personnel training
    • Medical, study & protocol specific, ICH-GCP

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