MENE RESEARCH

Mene Research has successfully executed over 150 phase trials in adherence to globally recognized standards like Good Clinical Practice (GCP), International Conference on Harmonization (ICH) principles, and pertinent national laws and regulations. This commitment ensures that all projects meet the highest ethical standards in the industry.
Blazing a trail in the clinical research landscape, Mene Research shines as the premier Contract Research Organization (CRO) in Turkiye to garner accreditation from the Turkish Medicine and Medical Device Agency. Our dynamic team excels in providing an extensive array of services for phase I to IV trials and medical device studies, encompassing:

  • Project Management
  • Regulatory and Site Start-up Management
  • Site Selection & Feasibility
  • Monitoring
  • Enrolment Boost
  • Quality Management
  • EDC & Data Management
  • Risk Management & Pharmacovigilance
  • Bioequivalence/Bioavailability Assessments

    With a track record of over 150 successfully executed phase trials, Mene Research adheres rigorously to internationally recognized benchmarks such as Good Clinical Practice (GCP), International Conference on Harmonization (ICH) principles, and relevant national legislation. This dedication ensures that all initiatives uphold the highest ethical standards prevalent in the industry ...