Clinical Monitoring

Veristat offers comprehensive clinical monitoring services from feasibility through site closeout to support clinical trials around the world.  Our clinical services are tailored to your needs, complimenting product development plans and overarching corporate and quality management policies. All monitoring activities are conducted in accordance with the study protocol, clinical monitoring plan, standard operating procedures, ICH GCP, and applicable regional regulations.

Explore Our Clinical Monitoring Services

Our clinical monitoring services are provided by qualified, knowledgeable professionals with extensive clinical research and therapeutic area experience. Veristat’s regional Clinical Research Associates (CRAs) have a minimum of 5 years of industry experience. You always have the opportunity to review CVs prior to approving monitoring personnel for your study. Veristat provides a clinical monitoring team that comprises both Veristat employees and trusted contractors, many of whom we have worked with for many years to provide the most effective and flexible solutions for each project. This approach provides our clients with a skilled and qualified therapeutically focused team.


Our Monitors Deliver


A Case Study

A Quick Feasibility Determines If the Study Can Expand into Europe

Veristat provides a feasibility assessment to a clinical stage biotechnology firm who wants to know whether it is feasible  to expand their current US study into European sites.



  • Site identification & selection
  • Site feasibility assessments
  • Site qualification & initiation
  • Budget and contract negotiations with sites
  • Ongoing site monitoring & management
  • Regulatory document collection, review & management
  • Management/facilitation of IRB/EC submissions
  • Remote monitoring via EDC
  • 100%, Targeted or Risk Based monitoring
  • Electronic Trial Master File management (eTMF)
  • Clinical Trial Vendor Management

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