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Medpace, Inc. is a contract research organization that works in partnership with leading pharmaceutical and biotech companies to bring promising new drugs to market. Medpace combines efficient clinical trial management with comprehensive regulatory consulting to provide sponsors with exceptional support during the drug development process. The integrated services at Medpace include: clinical development plan preparation, study management, regulatory document preparation, safety surveillance, clinical monitoring, medical imaging studies, data management, statistical analysis, medical writing, quality assurance auditing, comprehensive drug analysis, and US and international regulatory submissions. Medpace offers strategic guidance on the clinical development plan of a new product, development and submission of pre-IND and pre-NDA briefing packages, and preparation of the initial IND.