MCR Macro Clinical Research * Clinical Study Management * Monitoring * Regulatory and Government Affairs * Study Protocol Design * Preparation of Clinical Study Documentation * Investigator Recruitment * Subject Recruitment * Insurances * Drug and Biological Sample Logistics * Biostatistics and Data Management * Medical Writing * Quality Assurance Services * Health Economics * Preparation of Integrated Study Report * Archiving

Overview
MCR Clinical Research is a Contract Research Organization specialises in;
  • Clinical Study Management,
  • Monitoring,
  • Regulatory and Government Affairs


of all phases (I – IV) of clinical trials, ranging from small studies to complex, multinational projects in the best Turkish clinics fulfilling EMEA and FDA quality standards.

MCR Clinical Research offers the following services to global Pharmaceutical and Biotechnology companies involved in the clinical investigation of new drugs, new devices and new indications for existing drugs. These services are available separately or as part of a comprehensive clinical program. Our integrated Clinical Research services cover a wide range of activities from protocol development and site identification through completion of study reports. We try harder to complete every project fulfilling our sponsor's expectations in time and in budget.

  • Clinical Study Management
  • Monitoring
  • Regulatory and Government Affairs
  • Study Protocol Design
  • Preparation of Clinical Study Documentation
  • Investigator Recruitment
  • Subject Recruitment
  • Insurances
  • Drug and Biological Sample Logistics
  • Biostatistics and Data Management
  • Medical Writing
  • Quality Assurance Services
  • Health Economics
  • Preparation of Integrated Study Report
  • Archiving