Clinical Monitoring

Our Clinical Monitoring team is committed to delivering high-quality, responsive, and compliant oversight of investigator sites throughout the study lifecycle. We ensure that every site are complient to regulatory requirments.

What Sets Us Apart:

  • Highly Skilled CRAs

    • Every Clinical Research Associate (CRA) undergoes rigorous training and must demonstrate proven expertise in site monitoring before being assigned to any study.

  • Tailored Monitoring Plans

    • We offer 100% Source Document Verification (SDV) and Risk-Based Monitoring (RBM) strategies, customized to the study needs.

  • Comprehensive Visit Coverage

    • Our services includes sites activation, interim monitoring visits, and closeouts, ensuring efficient monitoring support.

  • Focused on Safety & Compliance

    • We monitor to identify the safety events ensuring patient safety and compliance at every stage of study conduct.

  • Continuous Improvement

    • Through ongoing refresher training programs and process improvisation, we keep our monitoring teams aligned with the latest in relevant guidelines & ICH GCP standards and industries best practices.

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During On-Site Visits, Our CRAs conduct the following:

  • Source data verification and Case Report Forms (CRFs) review for completeness & accuracy
  • Verify safety, regulatory and ethical compliance
  • Query management through proactive support to sites
  • Review and ensure study conduct is maintained through to final compliance
  • Support DSMB related data review and interim analyses as required