Quality Management
At Global MedTrial LLP, quality is not just a benchmark—it is embedded in every aspect of our clinical trial operations. Our comprehensive Quality Management System (QMS) ensures that all processes meet international standards and regulatory expectations, while promoting continuous improvement across our services.
Audit Program
We conduct structured and risk-based audits to evaluate the effectiveness and compliance of all trial-related activities.
Audit Planning
Annual Audits: Scheduled, comprehensive reviews of critical systems and processes.
Spot Checks: Unannounced audits to ensure day-to-day compliance.
Audit Scope
Annual Audits: Scheduled, comprehensive reviews of critical systems and processes.
Spot Checks: Unannounced audits to ensure day-to-day compliance.
We implement a proactive CAPA system to manage deviations and prevent recurrence of quality issues.
Key Activities:
- Coordinate and oversee the performance of Clinical Research Coordinators (CRCs).
- Identify, document, and investigate quality issues or non-compliance.
- Track resolution progress and ensure timely corrective actions.
- Monitor outcomes to confirm problem resolution and prevent future occurrences.
SOPs form the backbone of our operational integrity and regulatory compliance.
SOP Management:
- Regularly review and update SOPs to align with evolving regulations and best practices.
- Ensure all team members are trained and compliant with the latest SOP versions.
- Maintain thorough documentation and version control for audit readiness.
Our robust quality management practices enable us to deliver consistent, compliant, and high-quality clinical research support across every study we manage.
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