NCRG provides strategic regulatory consultation and clinical trial design and management for medical devices from concept through global market introduction in the fastest time possible. We provide expertise in the design, development and implementation of Quality Management Systems. NCRG has strong relationships with regulatory agencies and we serve as liaison for our clients through the regulatory and clinical process. NCRG staff implements effective project management throughout the regulatory and clinical processes while leveraging from the expertise of our partners around the world for monitoring, data management, statistical analyses and case support. NCRG will be certified to ISO 13485 in June, 2013.