The Clinical Research Service tailored to your need

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.

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.

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.

At Medex CRO, we are intensely working on our infrastructure that facilitates participant safety and regulatory compliance while providing efficiency that drives the growth of cutting-edge clinical research.

Mehmet YILDIZ • Founder of MEDEX GROUP

MEDEXERA is how we circulate information to our Sponsors, CRO, and SMO partners. We are preparing our SOPs through MEDEXERA, and advancing our sponsors' immediate needs and wants.

Anna GURLER • PM at Medex CRO

Medex as a Group has a unique expertise and capability in understanding the needs of global sponsors, CROs and also being open to working with other SMOs. We have a perspective to open up new kinds of opportunity both locally and globally

Sonila HOXHA • PM at Medex CRO

The Clinical Research Service tailored to your need

Clinical Operations

Regulatory

Data Management

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