CLINICAL MONITORING.
CLINICAL MONITORING.
IRES has a skilled clinical monitoring team with deep expertise in international GCP guidelines, delivering professional and innovative research support across all project stages.
The team excels in proactive communication, ensuring seamless collaboration with research teams and maintaining high-quality data management standards.
Our monitoring services comprehensively cover critical research lifecycle phases, including site visits, staff training, investigator meetings, and study termination procedures.
IRES combines technical proficiency with regulatory compliance, providing efficient and reliable monitoring solutions for complex clinical research projects.
SPECIFICS
ETHICS
Protecting patient rights and safety while in compliance with regulations and maintaining strict confidentiality.
pATIENT-CENTERED
Monitoring activities designed to minimize participant burden while maximizing their safety and study experience.
SYSTEMATIC
Structured approach to data collection and verification, following predefined monitoring schedules.
METHODOLOGY
Clear, consistent procedures for site visits, data review, and issue management based on risk assessment.
COMPREHENSIVE
Complete oversight of all critical study aspects, from consent documentation to endpoint data quality.
PRECISE
Accurate tracking of protocol deviations, meticulous source data verification, and detailed documentation of findings.