Clinical trial services

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IMR provides contract research organization (CRO) services to support your research initiative. Our services are following ICH, GCP and regulatory guidelines. IMR’s team key competencies include:

  • Study design;
  • Analysis and reporting of pre – clinical data;
  • Protocol development;
  • Case report form (CRF) design;
  • Development of investigator brochures and integrated summaries;
  • Site identification, pre-study feasibility;
  • Overall project management, identification of potential problems;
  • Site monitoring and management, liaisons to the sites; site regulatory documents collection;
  • Regulatory submission;
  • Safety data review and reconciliation of adverse events and serious adverse events;
  • Data management and statistical analysis of study data;
  • Organization of trainings;
  • Report writing etc.