Safety reporting is a critical component of clinical trial management. As a CRO, we are able to provide a full range of safety support services. Sponsors can rely on MedTrials to augment their internal teams or to manage medical monitoring, safety data review and regulatory reporting.
Services include:
- Medical consultation: reviewing and evaluating event collection and reporting, data analysis, clinical study reports (CSRs), and regulatory submissions
- Product safety: processing serious adverse event reports including evaluation of relatedness and analysis of similar events for expedited cases; identifying and evaluating safety signals, trends, and events
- Site education: training study teams on disease states, treatments, protocol compliance, inclusion and exclusion criteria, procedures, and assessments
- MedDRA coding
- Safety narrative development
- MedWatch reporting
Trial Management
MedTrials offers extensive clinical trial managemet expertise. We employ highly-trained clinical research professionals and deploy time-tested procedures to ensure you receive the right solutions for each study from start-up to close-out.
Learn MoreMonitoring
Highly trained and qualified clinical research associates (CRAs) ensure your sites are conducted, recorded, and reported in accordance with the study protocol and the applicable regulatory requirements.
Learn MoreSafety
Safety reporting is a critical component of clinical trial management. A partnership with MedTrials offers a full range of safety support services.
Learn MoreGrant Administration
Timely payment of investigators and study subjects directly correlates to clinical trial performance. MedTrials provides an end-to-end solution for clinical grants administration from budget negotiation and contracting.
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