MCR works in conformity to Good Clinical Practice (GCP) and current regulations. In addition MCR has developed a set of Standard Operating Procedures (SOPs) which are regularly updated to reflect regulatory environment. MCR offers a comprehensive set of services to provide medical devices and pharmaceutical companies with an integrated solution for product development and approval process. MCR has a large experience in investigator-initiated trials and can offer logistical and operational support, scientific and regulatory expertise and training.