Explore ARG’s Medical Monitoring services.Tell Us About Your Study
Every project is approached with clinical curiosity by asking, “What is important here in this particular study?
100% review of each ICSR, from source document analysis to query generation, and everything in between.
Formal review of each subject to ensure they meet inclusion/exclusion criteria prior to study enrollment.
Review of data listings to ensure accurate data is collected and improves subject safety by monitoring for signals.
Review of TLF mock-ups to proactively identify and mitigate potential issues, using our understanding of study data.
Review of coded terms to produce clean, consistent data, enabling timely database lock and better data representation.
Being involved in everything from protocol design to study planning, to trouble shooting problems as they arise, to the final steps of CSR review gives the Medical Monitoring team a unique perspective on the study and its data.