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Headquartered in the San Francisco Bay Area, RPI offers strategic and tactical regulatory expertise in all phases of drug development. RPI’s team of experts leverage our comprehensive submission experience to strategically position and guide clients through a streamlined and customized approach to achieve their drug development goals.
Our clients range from early-stage start-ups to some of the world’s largest life science companies and encompass all stages of product development, including pre-and post-approval settings. Our unique ability to create value as a trusted partner and as an integral member of existing scientific, regulatory and publishing teams have earned us our reputation as a solutions-oriented advisor providing support for regulatory activities in the US, Canada, EU and RoW.