Clinical Trial Monitoring & Site Management
From feasibility through site closeout, comprehensive clinical trial monitoring for studies around the world.
Veristat offers comprehensive clinical trial monitoring and site management services from feasibility through site closeout to support studies across regions and regulatory environments. Our services are tailored to your needs, complementing your product development plans and your corporate and quality management policies.
Our clinical trial monitoring and site management services are provided by qualified, knowledgeable professionals with extensive clinical research and therapeutic area experience.
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.
Veristat Expertise in Strategic Consulting
Experienced, Vetted CRAs
Veristat's regional Clinical Research Associates (CRAs) bring a minimum of 5 years of industry experience to every study. Clients can review CRA CVs before approving monitoring personnel, so you know exactly who is overseeing your data and your sites.
Full Site Lifecycle Management
Our teams manage every stage of the site relationship, from feasibility assessments and site identification through qualification, initiation, budget and contract negotiations, ongoing monitoring and management, and site closeout.
Consistent, Audit-Ready Standards
Every activity follows the study protocol, the clinical monitoring plan, standard operating procedures, ICH GCP, and applicable regional regulations, giving sponsors a reliable, audit-ready standard of oversight across every site.
Site feasibility assessments
Evaluating site readiness and capability before commitment Site identification & selection.
Finding and selecting the right sites for your trial.
Site qualification & initiation.
Getting sites qualified and up and running.
Ongoing site monitoring & management.
Continuous oversight throughout the life of your trial.
Regulatory document collection, review & management.
Keeping site regulatory documentation complete and current.
IRB/EC Submission Management.
Facilitating submissions to Institutional Review Boards(IRB) and Ethics Committees (EC).
Remote monitoring via EDC.
Where available, monitoring capability that doesn't require an on-site visit.
100%, Targeted or Risk Based monitoring.
Choosing the right monitoring intensity for your study's needs.
Electronic Trial Master File management (eTMF).
Keeping your trial documentation organized and inspection-ready.
NEXT STEPS
What's Next in the Drug Development Process
Patient Retention & Site Engagement
Keep enrolled patients and engaged sites through to study completion. Utilizing partner platforms to enhance the patient journey and reduce the burden.
Project Management.
Ensure your monitoring activities stay aligned with budget and timeline.
See what’s happening where it matters most.
Your sites are where trial performance becomes visible. Veristat’s monitoring experts bring site activity, data quality, protocol adherence, and emerging risks into focus, giving your team the information it needs to address issues early and make informed decisions that keep the study moving forward.
Frequently Asked Questions
Veristat's regional Clinical Research Associates (CRAs) have a minimum of 5 years of industry experience, and clients can review CRA CVs before approving monitoring personnel for their study.
100% source data verification reviews all trial data against source documents, while risk-based monitoring focuses review efforts on the areas of highest risk to patient safety and data integrity, Veristat offers both approaches depending on what a study needs.
Yes. Veristat provides remote monitoring via EDC where available, allowing oversight without requiring an on-site visit for every review.