Gail H. Javitt

Gail H. Javitt

FDA Law

5.0 (1 reviews)
Washington, District of Columbia
Hyman, Phelps & McNamara PC
Updated:

Contact Information

1101 K Street, NW, Suite 700, Washington, DC 20005
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Bio

Ms. Javitt provides strategic FDA regulatory advice for leading medical device, diagnostics, pharmaceutical, biological products, and human cellular, and tissue-based products (HCT/Ps) throughout the product life cycle and has successfully resolved disputes at both the pre- and post-market stage. She also has significant experience advising clinical laboratories on FDA and CLIA requirements for laboratory developed tests.Ms. Javitt’s experience prior to joining Hyman, Phelps & McNamara includes serving as a partner in a leading Washington, DC health law practice and as a law and policy director at the Genetics and Public Policy Center, part of Johns Hopkins University. At the Center, she was responsible for developing policy options to guide the development and use of reproductive and other genetic technologies. Earlier in her legal career, Ms. Javitt clerked for the Honorable Gary Taylor of the U.S. District Court for the Central District of California.In addition, Ms. Javitt has published and spoken widely on issues at the intersection of law, science, ethics and policy, including FDA regulation of genetic testing, precision medicine, and next-generation sequencing. Her academic experience has included serving as a faculty member at the Berman Institute of Bioethics at Johns Hopkins University and as an adjunct professor at the Georgetown University Law Center, American University’s Washington College of Law, and the University of Maryland School of Law. She was previously a Greenwall Fellow in Bioethics and Health Policy, a collaborative effort between Johns Hopkins University and Georgetown University Ms. Javitt provides strategic FDA regulatory advice for leading medical device, diagnostics, pharmaceutical, biological products, and human cellular, and tissue-based products (HCT/Ps) throughout the product life cycle and has successfully resolved disputes at both the pre- and post-market stage. She also has significant experience advising clinical laboratories on FDA and CLIA requirements for laboratory developed tests.Ms. Javitt’s experience prior to joining Hyman, Phelps & McNamara includes serving as a partner in a leading Washington, DC health law practice and as a law and policy director at the Genetics and Public Policy Center, part of Johns Hopkins University. At the Center, she was responsible for developing policy options to guide the development and use of reproductive and other genetic technologies. Earlier in her legal career, Ms. Javitt clerked for the Honorable Gary Taylor of the U.S. District Court for the Central District of California.In addition, Ms. Javitt has published and spoken widely on issues at the intersection of law, science, ethics and policy, including FDA regulation of genetic testing, precision medicine, and next-generation sequencing. Her academic experience has included serving as a faculty member at the Berman Institute of Bioethics at Johns Hopkins University and as an adjunct professor at the Georgetown University Law Center, American University’s Washington College of Law, and the University of Maryland School of Law. She was previously a Greenwall Fellow in Bioethics and Health Policy, a collaborative effort between Johns Hopkins University and Georgetown University Ms. Javitt clerked for the Honorable Gary Taylor of the U.S. District Court for the Central District of California. In addition, Ms.

Practice Areas

FDA Law

Awards & Recognition

  • Recognized: FDA Law

Recognized in Best Lawyers since 2025

Education

  • Columbia University, B.A.
  • Harvard University, J.D.

Reviews

A

Anna Wright

2 months ago

Invaluable FDA Regulatory Guidance for Our New Medical Device

Our company was navigating the complex pre-market submission for a novel diagnostic device, and Gail Javitt was instrumental in our success. Her deep knowledge of FDA regulations, particularly for diagnostics and medical devices, is exceptional. She provided clear, strategic advice that went beyond simple compliance, helping us structure our clinical data to best address agency concerns. Her background from a top-tier firm and recognition in FDA law were evident in every interaction. Thanks to her guidance, we received clearance without significant delays. Gail is a true expert who combines professionalism with practical, business-focused counsel.

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