Courtenay C. Brinckerhoff
Socio
Courtenay Brinckerhoff es abogada especializada en propiedad intelectual y asesora a clientes internacionales en todos los aspectos relacionados con la obtención, defensa, evaluación, concesión de licencias y aplicación de patentes, además de llevar a cabo investigaciones sobre libertad de operación y diligencia debida. Es socia y vicepresidenta del Departamento de Propiedad Intelectual del bufete, así como editora y autora principal de Foley'sPharmaPatentsBlog.com, donde analiza la evolución de las prácticas de las oficinas de patentes y las sentencias judiciales sobre cuestiones jurídicas emergentes.
For more than 25 years, Courtenay has represented clients in diverse industries before the U.S. Patent Office, the Patent Trial and Appeal Board, and the U.S. Court of Appeals for the Federal Circuit. She has successfully represented clients in complex patent matters, including four-party interference, Inter partes Reexaminations, Inter partes Reviews, and ANDA litigation.
Courtenay works with clients across the chemical and biotechnology industries, including on innovations for pharmaceuticals and drug-device products, human and animal food products and nutraceuticals, and industrial technologies. Clients trust Courtenay to secure critical intellectual patent rights, including patents intended for listing in the Orange Book or eligible for listing in the Purple Book.
She has particular experience with transdermal pharmaceutical products (patches, gels, and liquids), oral dosage forms (including controlled/extended-release formulations), enzyme-based technologies, microbial technologies, diagnostic and therapeutic antibodies, active and passive immunization therapies, and personalized medicine, as well as with industrial films, carbon nanotube technologies, biofuels, and carbon capture technologies.
Courtenay has served as vice chair of the firm’s Chemical, Biotechnology & Pharmaceutical Practice and is an active member of the firm’s PTAB Trials Practice and Life Sciences Industry Team.
Prior to joining Foley as an associate, Courtenay clerked for the Honorable Alvin Anthony Schall on the U.S. Court of Appeals for the Federal Circuit. Prior to her clerkship, she worked at Foley as a patent agent and law clerk.
Premios y reconocimientos
- Stand-out Lawyer, Thomson Reuters (2025)
- The Best Lawyers in America©, Patent Law (2021-2024) and Biotechnology and Life Sciences Practice (2023-2024)
- IP Distinguished Alumni Award from George Mason University Antonin Scalia Law School (April 2017)
- JD Supra Readers’ Choice Top Author (2017-2021) in the categories of pharmaceutical industry and patents for her work on the PharmaPatents blog
- IAM Patent 1000 – The World’s Leading Patent Practitioners, patent prosecution (2014-2016, 2020-2021, 2024-2025)
- Top Women in IP, Managing IP (2015)
- IP Star, Managing IP (2015)
Liderazgo intelectual
Courtenay writes and speaks on topics important to clients in chemical, biotechnological, pharmaceutical, food, and personalized medicine industries. She has been an invited speaker at the AIPLA Annual Meeting, the FDLI Annual Meeting, the Intellectual Property Owner’s Association annual meeting, the PTAB Bar Association annual meeting, and the annual Advanced Patent Law Institute presented by the University of Texas School of Law, the United States Patent and Trademark Office, and George Mason University Antonin Scalia Law School.
Courtenay currently serves as a Vice Chair of the Intellectual Property Owner’s Association Patent Office Practice Committee and as a Vice Chair of the Appeals to the PTAB Committee of the PTAB Bar Association.
Courtenay has been following U.S. patent reform since its inception, and she and other Foley colleagues co-authored the treatise, America Invents Act: Law & Analysis (Wolters Kluwer 2012). The interface between patent law and FDA law is another area of interest, and she has written and spoken on issues including patent term extension, the scope of the Hatch-Waxman “safe harbor,” the ANDA litigation framework, and the biosimilars BPCIA framework.
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El Director de la USPTO toma el control de las decisiones institucionales en materia de DPI y RGP
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La USPTO publica una propuesta de reglamento sobre denegaciones discrecionales de procedimientos IPR
¿Ayudará a la USPTO a probar la búsqueda del estado de la técnica generada por IA?
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