Phase II-IV

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Phase II-IV Studies at Synchron Research

We conduct

  • FIRST-INTO MAN STUDIES
  • FEASIBILITY STUDY
  • PROTOCOL DEVELOPMENT
  • SITE IDENTIFICATION
  • CLINICAL INVESTIGATOR SELECTION
  • CLINICAL STUDY MONITORING
  • CLINICAL TRIAL CO-ORDINATION
  • CLINICAL TRIAL PROJECT MANAGEMENT
  • INDEPENDENT ETHICS COMMITTEE SUBMISSION
  • REGULATORY SUBMISSIONS
  • POST MARKETING SURVEILLANCE

Our GCP trained personnel are competent to carry out the above functions which meet International standards. All project management activities are carried out in compliance with ICH and GCP guidelines.