IMR provides contract research organization (CRO) services to support your research initiative. The institute offers a full service spectrum for clinical trial conduction. Our services are following ICH, GCP, and regulatory guidelines, guaranteeing our reliability as a partner and service provider. 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.