Mene SMO able to resourcing Clinical Research Coordinators (CRC). All Mene SMO CRCs are  experienced and specialized research professional working with and under the direction of PI. CRC suppor


WAREHOUSING/LOGISTICS/ SOURCING ( DEPOT MERIDIAN) licensed in Turkey to purchase medical products required as comparators/ Concomitant/ rescue medications for a clinical trial 8680713050015


Mene Research is a clinical research organization operating in USA, Europe and Middle East, running activities including managing all the processes from early phase to late phases and evaluating the outputs of these processes; determining development strategies starting from the discovery of the molecule and invention of the medical device. MENE Research has become the first trials group to be accredited by the country’s Ministry of Health under new trial laws introduced in January, 2009

MENE Research has a reliable, experienced and qualified team of people from different medical backgrounds who perform in a timely and cost effective manner. Our team has the expertise and the know-how to satisfy the needs of your company/center/hospital, quickly and professionally.

MENE Research combines the advantages of a midsize CRO with local presence and local expertise. Flexibility, dynamism, personal dedication, simple company structure local knowledge enables Mene Research to offer high value for money services.

Our clients are local and multinational pharmaceutical companies, medical centers, health funds, doctor’s associations, collaborating CROs, and others.

Our company also runs in compliance with the International Conference on Harmonization (ICH), principles of Good Clinical Practice (GCP) and according with the national, international laws, and business ethics.



Group of professionals with over 150 years combined experience working the field of medical device development, evaluation and review. Most of our associates are former employees of the U.S. Food and Drug Administration and/or industry regulatory affairs professionals. CardioMed focuses on cardiovascular implants, including bare and drug eluting coronary and peripheral stents, endovascular grafts, heart valves, heart failure devices, and other novel and first-of-a-kind devices.

CardioMed’s services including regulatory consulting services, engineering consulting services, quality systems consulting services, customized training programs, and clinical trial services. Our clinical trial services team can provide trial design, full protocol development, medical writing, data analysis, and reporting.

Our team of professionals have the education, experience, and broad knowledge of FDA’s processes and requirements to assist both large companies and entrepreneurial startups through the regulatory process.