Clinical Monitoring : keeping trials on track   

Qtech solutions have core expertise in clinical research monitoring and we have assembled a strong team of Clinical research professionals. Our Clinical research team provide our clients with local expertise and responsive staff dedicated to their projects that will ensure protocol compliance and accurate data collection for your study - they are professional, efficient, and act as a seamless extension of your organization. They work closely with Data Management groups to form a specialized Data Collection Team for each study. Qtech Solutions can provide all types of clinical monitoring from pre-study, site initiation, interim, to site close-out. Qtech offers flexible clinical monitoring services, designed to accommodate any type or phase of a clinical trial. We can deliver experienced professionals—individuals or entire teams—to monitor all aspects of a clinical trial or simply to fill critical knowledge or experience gaps in your team. If you need a complete monitoring team, we can provide one with the right background and experience for your specific needs. Our experienced clinical research professionals can easily integrate with your in-house clinical team to manage local trials or you can take advantage of the Qtech national network of clinical research professionals for trials requiring regional monitoring. Whether your clinical trials are conducted locally, regionally, nationally, or worldwide, we can provide you with the proven professionals you need

Site Initiation

    • Research site selection and evaluation.
    • Investigators’ meeting.
    • Personnel training.
    • Site initiation.
    • Site set-up and training for (EDC) Electronic Data Capture.

Site Monitoring

  • Source data verification.
  • Checking internal consistency of CRF data.
  • Data query management.
  • Issuing Data Alerts to CDM.
  • Monitoring of enrollment rate and patient eligibility criteria.
  • Drug accountability.
  • Site closure.
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