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
Depot Meridian (a subdivision of Mene Research) is the first inspected and approved clinical trial specific warehouse by Turkish Medicines and Medical Devices Agency. Depot Meridian allows clients to demonstrate effective compliance with regulatory requirements by providing a full documented chain of custody for every medication unit, from dispatch, dispensing, to destruction. Depot Meridian warehousing services could be offered either as a part of clinical trials services (through Mene Research) or as a standalone service.
Established in January 2003, CardioMed Device Consultants is an expanding group of professionals with over 100 years of combined experience working in the field of medical device development, evaluation, and review. Many of our principal members are former employees of the U.S. Food and Drug Administration’s (FDA) Center for Devices and Radiological Health (CDRH). They have had integral roles in the review of medical device marketing applications and regulatory submissions, the development of FDA guidance documents, FDA policies, and both U.S. and international voluntary performance standards.
Flex Databases is offering CTMS (Clinical Trial Management System), Project Management and Budgeting, LMS (Learning Management System), TMF (Trial Master File), EDC (Electronic Data Capture), IWRS (Interactive Web Response System), Corporate Portol infrastructure to its clients.