We support Bioequivalence studies in seven BE/BA inpatient units in Turkey, Jordan, Egypt and Tunisia. Our Bioequivalence operation is led by multi-disciplinary committee that covers study design, protocol writing, statistical analysis, regulatory approval and any necessary services for your submission.

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We can arrange for full service study or limited support to any of the clinical or analysis and reporting part of your project.  Our staff brings to your company extensive experience and your studies will be conducted in certified facilities following regulatory guidelines and regulations.