Expert medical monitoring is crucial for streamlining clinical research. An integrated approach will improve outcomes while ensuring trial subject safety.
We offer unrivaled expertise in medical monitoring services, providing tailored solutions in accordance with study specifications and requirements. Our safety physicians have extensive knowledge of a broad range of therapeutic areas and will support essential project oversight and procedure clarity, enabling close interaction with key partners and timely delivery of evaluations. We also offer support for smooth patient recruitment, ensuring safety and helping you to define and qualify inclusion/exclusion criteria.
Our experts provide high-quality medical review services for study protocols, clinical study reports, review and approval of MedDRA and ATC codes, as well as medical reviews of a wide range of safety data, including adverse effects (AEs) and serious adverse effects (SAEs) reported in the clinical and/or safety database. Additional services include independent medical monitoring for safety review meetings and participation in Independent Data Monitoring Committees (IDMCs) and Data Safety Monitoring Boards (DSMBs).
SGS is recognized as the benchmark for quality and integrity in clinical research. We are your first choice when looking for exceptional customized medical monitoring for your research project.