I. Nonclinical and Clinical Services:

  • Pharmacology and Toxicology Studies
  • Feasibility Studies
  • Bioavailability and Bioequivalence Studies
  • Phase I-IV Clinical Trials
  • Pharmacovigilance / Drug Safety Studies
  • Safety and Efficacy Studies (for Non-Drug Products)
  • Site Initiation and Activation
  • Patient Recruitment
  • Clinical Trial Monitoring and Management
  • Data Management
  • Biostatistics
  • Quality Control and Compliance
  • Medical and Clinical Trial Report Writing

II. Consultancy Services:

  • Drug / Product Development Strategy
  • Clinical Trial Planning, Design and Strategy
  • Regulatory and Compliance Affairs
  • Research Project Management