Clinical Research Consultants, Inc. provides consulting services in the fields of regulatory affairs (including preparation of IDE, PMA and 510K submissions to the FDA), clinical trials management, quality systems regulations and quality systems management, manufacturing systems, operations, and strategic planning as they relate to research and development of medical devices and related technology

The collaborative member consultants of Clinical Research Consultants, Inc. each have in excess of 20 years of experience in their respective fields of pharmacy, medical devices, engineering, and business operations. They have a unique blend of experience in venture capital funding that enables them to integrate the research and development efforts with the desired business strategy for their various U.S. and international based clients and projects.