Site Management Services

The performance of study sites is not only critical to the success of any clinical research project, it is the single most important factor.
Keeping this in mind, for the physicians who have a large patient population and are interested in expanding their private practice/clinic into clinical research field as an investigative site, we offer following services to help prepare the sites ready to conduct the clinical trials.

Our Services Include

Therapeutic Specific Studies


Contract/Budget Negotiation

Regulatory Documentation

IRB approvals

Preparing for Monitoring Visits

Site Staff Training

Site/Subject Payments

EDC/IVRS Training

Source Documentation

Data Entry

Lab Sample Processing & Handling

Site Audits & Inspection Readiness

Contact Info

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