Eric Greig

About Eric Greig

Partner in the Washington, D.C. office of Cooley LLP. Advises clients on healthcare regulatory matters, market access strategies, and reimbursement issues across the medical device, pharmaceutical, digital health, biotechnology, clinical laboratory, and healthcare services sectors.Leverages track record of successes in bet-the-company regulatory matters, as well as extensive experience with health payment systems and innovative solutions, to guide clients across the healthcare and life sciences industry on:• Development and execution of market access strategies for new and existing technologies• Advocacy with Congress and federal and state agencies, including the Centers for Medicare and Medicaid Services (CMS)• Medicare and Medicaid coverage, coding, and reimbursement matters• Compliance with billing policies• Federal and state fraud and abuse laws, including development of compliance programs• Federal and state “sunshine” laws• Complex litigation matters, including government audits and investigations, qui tam lawsuits, and other matters involving the HHS Office of Inspector General (OIG), US Department of Justice, and CMS Center for Program IntegrityAlso advises private equity firms, investment banks, venture capital funds, commercial lenders, and healthcare and life science companies on regulatory issues related to mergers and acquisitions, IPOs, and US financings.A member of the American Health Law Association and the American Bar Association Health Law Section. A recognized thought leader, regularly writes and speaks on healthcare and life sciences topics. Co-authored a chapter related to Medicare and Medicaid reimbursement for off-label uses of drugs and devices in Off-Label Communications: A Guide to Sales & Marketing Compliance, published by the Food and Drug Law Institute (FDLI), and presents on healthcare regulatory and reimbursement topics at national conferences organized by leading industry organizations including AdvaMed, PhRMA, the American Health Law Association (AHLA), the Medical Device Manufacturers Association (MDMA), the 8400 Health Network, and the California Life Sciences Institute.Portions of this profile may constitute attorney advertising. Any testimonial or endorsement on this profile does not constitute a guarantee, warranty, or prediction regarding the outcome of your legal matter. Prior results do not guarantee a similar outcome.

Experience

1. Partner

   Cooley LLP

   Apr 2025 — Present · Washington, DC, US

Education

• The University of Texas School of Law

  Doctor of Law (J.D.)

  2007 — 2010

• The Ohio State University

  Bachelor of Science (BS), Microbiology and Philosophy; Minor in Communications

  2002 — 2006