Advantage vedic

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  • Protocols aligned with your marketing goals
  • Laser sharp selection of most suitable assessment tools
  • Clear, transparent and customer-centric costing process with built-in guarantees
  • Rapid study start-up thanks to faster recruitment from ready pool of volunteers, spread across multiple clinical sites
  • Microfine control of sensitive aspects at investigational sites, especially in placebo-controlled studies using Patient Reported Outcome Measures (PROMs)
  • GCP compliant processes, documentation and triple layered quality control of data
  • Costs up to 40% lower than comparable CROs anywhere in the world
  • Real-time access to project status reports and study data
  • Credible, accurate and professional clinical study reports acceptable to global regulatory bodies and scientific journals
  • High probability of publications and approvals
  • Early intimation of trends to facilitate change of course if required


  • Protocol Planning

  • Project Management

  • Site(s) Initiation

  • Clinical Monitoring

  • Data Management

  • Study Publication