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Provided by Nikki Reeves
Nikki Reeves is an FDA and healthcare regulatory compliance lawyer with more than 25 years of experience. Nikki co-chairs the firm's Government Matters & Regulatory practice management group, which is comprised of 200+ lawyers and consultants in eight practice areas. Nikki previously co-chaired the firm’s Life Sciences and Healthcare Industry Group for six years, which is comprised of more than 450 lawyers across seventeen practice areas in the firm.
As Deputy Chair of the firm's FDA & Life Sciences practice, Nikki advises pharmaceutical and medical device companies on pre- and post-market FDA regulatory compliance and enforcement matters ranging from clinical trials, good manufacturing practices, to labeling, advertising, and promotion of FDA-regulated products. Nikki has been the lead FDA regulatory advisor to her clients on 250+ transactional matters. She conducts investigations into FDA clinical trials and post-marking noncompliance, acts as lead compliance and regulatory counsel for several companies under Corporate Integrity Agreements (CIAs) and has led several CMS Open Payments compliance audits.
Ms. Reeves is an expert on federal Open Payments, state, and international transparency/disclosure laws and leads two pharma and device industry compliance coalitions.
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Nikki is incredibly business savvy and brings a highly valuable perspective about the industry to the table.
Nikki is incredibly business savvy and brings a highly valuable perspective about the industry to the table.