Medpoint offers distinctive consulting services in the areas of quality assurance and regulatory and clinical affairs. Our global network of subject matter experts are strategically placed around the world working all levels of projects in Medical Device, Biotech, and Pharmaceutical in over 90 countries. Medpoint's clients span the spectrum from start-up to Fortune 20 and look to Medpoint for short-term or long-term expertise and encompass areas from FDA/ISO Guidance to Risk Analysis and Management to Biologics. From ensuring that your quality management system complies with regulations and standards, to facilitating new product introduction, to explaining best practices and guidelines, we make sure that your company is where it needs to be. ISO 9001: 2015 Certified