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Managing study sites
Proper site management is an essential factor in executing a clinical trial successfully. Site management is much more than simply monitoring a study site, it’s about developing a solid working relationship with the site through regular and consistent communication.
Trust and support
Medicorent understands the central role that sites play in the outcome of a clinical study. We establish a trust-based relationship with each site, maintaining an appropriate level of oversight and supporting the study personnel throughout all phases of the clinical study. Because our own experiences, we understand first-hand the daily pressures that study personnel face to balance clinical research with their routine clinical responsibilities. That’s why we strive to simplify their work when possible and to support them in any way we can.
Facilitation and review of enrollment
Regular communication with sites
Ensuring regulatory compliance and adherence to the clinical study protocol
Trial Master File (TMF) creation and maintenance
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