John D. Shakow

Practice Areas

John Shakow's practice focuses on complex regulatory, commercial, investigation and litigation issues related to pharmaceutical government pricing and price reporting. As a partner in the FDA and Life Sciences practice, he represents pharmaceutical and biotechnology manufacturers in every facet of government drug payor program compliance. John has 20 years of experience in helping pharmaceutical and biotechnology clients resolve commercial and organizational challenges while maintaining the integrity of their price-reporting compliance efforts.

Mr. Shakow often conducts in-depth pricing assessments to develop and implement government price calculation and reporting policies, procedures, systems and methodologies. John has overseen over a dozen substantial bona fide service fee analysis projects for large and small drug manufacturers. He is experienced in managing the coordination and integration of pricing methodologies in major pharmaceutical mergers.