FacultyFaculty/Author Profile

Christopher Pruitt

Covington & Burling LLP

Washington, DC, USA


CHRISTOPHER H. PRUITT
Associate

Christopher Pruitt is an associate in the firm's Washington, DC office in the Food & Drug and Government Contracts practice groups. He has experience advising manufacturers of drugs, devices, food, and other products on a range of regulatory issues involving the Food & Drug Administration, including compliance, transactional, and enforcement matters. Mr. Pruitt has particular experience with legal and regulatory issues related to FDA regulation of medical device software, promotion in social media, in vitro diagnostics, regulation of clinical laboratories, and food safety. Mr. Pruitt also advises drug and device manufacturers of legal and regulatory obligations associated with selling products to the Federal Government.

REPRESENTATIVE MATTERS

  • Evaluated software and mobile medical applications for compliance with FDA medical device regulations and policies.
  • Represented a pharmaceutical manufacturer in an administrative hearing before FDA challenging a refusal to approve a supplemental application.
  • Represented a pharmaceutical manufacturer in litigation challenging approval of a generic product.
  • Co-authored a U.S. Supreme Court amicus brief on preemption of tort claims regarding the labeling of over-the-counter medicines.
  • Provided strategic regulatory advice to pharmaceutical manufacturers evaluating companion diagnostic opportunities.
  • Co-authored a successful Citizen Petition that advocated for FDA to exempt the storage of packaged foods from hazard analysis and preventive controls requirements.
  • Represented a clinical laboratory challenging sanctions imposed by the Centers for Medicare and Medicaid Services for alleged violations of the Clinical Laboratory Improvement Amendments.
  • Advised pharmaceutical and medical device manufacturers on operating procedures and policies regarding promotion of products on internet and new media.
  • Advised pharmaceutical manufacturers of compliance obligations related to the Federal Awardee Performance and Integrity Information System.

Practices

  • Food & Drug
  • Government Contracts

Industries

  • Life Sciences

Education

  • George Mason University School of Law, J.D., 2007
    • magna cum laude
    • George Mason Law Review, Symposium Editor
  • Pennsylvania State University, B.A., 2004
    • Political Science
    • Minor in Economics
    • with highest distinction
    • Phi Beta Kappa

Judicial Clerkship

  • Hon. Patricia C. Fawsett, U.S. District Court, Middle District of Florida, 2007-2009

Bar Admissions

  • District of Columbia
  • Virginia
Share
Email

  • FOLLOW PLI:
  • twitter
  • LinkedIn
  • GooglePlus
  • RSS

All Contents Copyright © 1996-2017 Practising Law Institute. Continuing Legal Education since 1933.

© 2017 PLI PRACTISING LAW INSTITUTE. All rights reserved. The PLI logo is a service mark of PLI.