The integrated services at Medpace include: clinical development plan preparation, project management, regulatory document preparation, safety surveillance, clinical monitoring, data management, statistical analysis, medical writing, quality assurance auditing, and US and international regulatory submissions. At Medpace, proven leaders in medical and scientific research monitor every project. The therapeutic focus and experience of the Medpace team, which includes on-staff physicians, reduces the need for client oversight, review, and training. In addition, Medpace physicians have first-hand experience working with regulatory agencies to successfully guide projects through the complexities of the regulatory process. The medical expertise and regulatory guidance provided by Medpace leads