The Clinical Research Service tailored to your need
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Clinical Operations
Through meticulous planning and organization supported by targeted SOPs. We are here to help, from study design, protocol development and completion of a series of clinical trial documentation to regulatory approvals and training study teams and sites, monitoring and site relationships.
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Regulatory
Since 2017, we have been successfully fulfilling the requirements of the regulatory systems of the Ministry of Health Turkey, FDA, and EMA.
We have extensive experience of regulatory document preparation together with the management of client-focused projects with a strong record of successful outcomes.
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Data Management
MEDEX CRO
provides traditional clinical data management solutions as well as an Electronic Data Capture (EDC) and Electronic Patient Reported Outcomes (ePRO) approach, giving flexibility in data management solutions while always maintaining high standards for data quality and timeliness.
Our References
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