Clinical Research & Monitoring

We provide comprehensive support in clinical research and trial monitoring to ensure data integrity, participant safety, and regulatory compliance. Our expertise covers protocol adherence, source data verification, risk-based monitoring, and central oversight, helping sponsors and research teams achieve high-quality results while meeting ICH-GCP and regulatory requirements. By combining technology with hands-on experience, we streamline research operations and strengthen the reliability of study outcomes.

We provide the following products…

Site Monitoring & Compliance Audits

    • Description: On-site or remote monitoring visits to verify protocol adherence, informed consent, and source data accuracy. Includes compliance checks and corrective action plans.

    • Format: Visit-based service (per monitoring visit or audit).

  • Pricing Plans:
    • Starter – $600/visit
      Basic site visit with monitoring report.
    • Pro – $1,200/visit
      Full monitoring visit with compliance checks and action plan.
    • Premium – $2,000+/visit
      Comprehensive monitoring & audit package with detailed CAPA (Corrective & Preventive Actions).

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Risk-Based & Centralized Monitoring

    • Description: Data-driven monitoring solutions that identify trends, outliers, and risks early. Combines centralized review with targeted site monitoring to optimize resources while ensuring quality.

    • Format: Ongoing service with monthly/quarterly reports.

  • Pricing Plans:

    • Starter – $400/month
      Central monitoring with basic data review.

    • Pro – $900/month
      Advanced risk-based monitoring with dashboards and site feedback.

    • Premium – $1,800+/month
      Full central monitoring service with analytics, reporting, and integrated oversight.