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| Medical Monitoring & Adverse Event Reporting |
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TrialMed has a comprehensive training program provides consistent training in Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs)/International Conference on Harmonization (ICH) Guidelines, and regulatory requirements across regions.
We make sincere effort to work with the sponsor company to report and document adverse event, serious adverse events and un-anticipated adverse events.
Our monitors have medical knowledge and are trained to monitor documents, understand patients' histories and guide the sites to document.
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