Chesterfield Smith Eminent Scholar Chair
Professor of Law
Constitutional Law and Civil Rights • Medical Technology • Public Health Law • S.T.E.M. subjects • Tort Law •
Lars Noah is the Chesterfield Smith Eminent Scholar Chair and Professor of Law at the University of Florida, where he has taught courses in Administrative Law, Medical Technology, Public Health Law, and Torts, among other subjects. Professor Noah has published more than seventy scholarly articles on a wide range of subjects as well as a casebook that focuses on the regulation of pharmaceuticals and medical devices: Law, Medicine, and Medical Technology (Foundation Press 5th ed. 2022). As something of a bookend to that volume, Professor Noah has now also penned (again unaided) Law and the Public’s Health: Cases, Controversies, and Covid-19 (Carolina Academic Press 2023). He has served as a visiting professor at Georgetown, Texas, Vanderbilt, George Washington, U.C. Hastings, and Washington & Lee, and he has worked with expert committees at the National Academy of Sciences and the National Institutes of Health. Before entering academia in 1994, Professor Noah clerked for Chief Judge Abner J. Mikva on the U.S. Court of Appeals for the D.C. Circuit and then practiced law for three years at Covington & Burling in Washington, D.C.
J.D., Harvard University (magna cum laude)
B.A., Harvard University (magna cum laude)
- Medical Technology
- Public Health Law
- LAW AND THE PUBLIC’S HEALTH: CASES, CONTROVERSIES & COVID-19 (Carolina Academic Press 2023)
- LAW, MEDICINE, AND MEDICAL TECHNOLOGY: CASES & MATERIALS (Foundation Press 5th ed. 2022)
- LAW, MEDICINE, AND MEDICAL TECHNOLOGY: CASES & MATERIALS (Foundation Press 4th ed. 2017)
- LAW, MEDICINE, AND MEDICAL TECHNOLOGY: CASES & MATERIALS (Foundation Press 3d ed. 2012)
- LAW, MEDICINE, AND MEDICAL TECHNOLOGY: CASES & MATERIALS (Foundation Press 2d ed. 2007)
- LAW, MEDICINE, AND MEDICAL TECHNOLOGY: CASES & MATERIALS (Foundation Press 2002)
- Time to Bite the Bullet?: How an Emboldened FDA Could Take Aim at the Firearms Industry, 53 Conn. L. Rev. 787 (2022).
- Censorship Is So Last Century: Therapeutic Products, Propaganda, and Compelled Speech, 66 St. Louis U. L.J. 79 (2021).
- State Regulatory Responses to the Prescription Opioid Crisis: Too Much to Bear?, 124 Dick. L. Rev. 633 (2020).
- Banning Off-Label Drug Promotion Offends the U.S. Constitution: Making the Strongest Case, 83 Alb. L. Rev. 301 (2020).
- Does the U.S. Constitution Constrain State Products Liability Doctrine?, 92 Temp. L. Rev. 189 (2019).
- Federal Regulatory Responses to the Prescription Opioid Crisis: Too Little, Too Late?, 2019 Utah L. Rev. 757 (2019).
- Giving Personal Injury Attorneys Who Run Misleading Drug Ads a Dose of Their Own Medicine, 2019 U. Ill. L. Rev. 791 (2019).
- Doctors on the Take: Aligning Tort Law to Address Drug Company Payments to Prescribers, 66 Buff. L. Rev. 855 (2018).
- Reversal of Fortune: Moving Pharmaceuticals from Over-the-Counter to Prescription Status?, 63 Vill. L. Rev. 355 (2018).
- “Go Sue Yourself!” Imagining Intrapersonal Liability for Negligently Self-Inflicted Harms, 70 Fla. L. Rev. 649 (2018).
- When Constitutional Tailoring Demands the Impossible: Unrealistic Scrutiny of Agencies?, 85 Geo. Wash. L. Rev. 1462 (2017).
- State Affronts to Federal Primacy in the Licensure of Pharmaceutical Products, 2016 Mich. St. L. Rev. 1 (2016).
- Growing Organs in the Lab: Tissue Engineers Confront Institutional “Immune” Responses, 55 Jurimetrics J. 297 (2015).
- Product Hopping 2.0: Getting the FDA to Yank Your Original License Beats Stacking Patents, 19 Marq. Intell. Prop. L. Rev. 161 (2015).
- Governance by the Backdoor: Administrative Law(lessness?) at the FDA, 93 Neb. L. Rev. 89 (2014).
- Permission to Speak Freely?, 162 U. Pa. L. Rev. Online 248 (2014).
- Genetic Modification and Food Irradiation: Are Those Strictly on a Need-to-Know Basis?, 118 Penn. St. L. Rev. 759 (2014).
- Turn the Beat Around?: Deactivating Implanted Cardiac-Assist Devices, 39 Wm. Mitchell L. Rev. 1229 (2013).
- Whatever Happened to the “Frankenfish”?: The FDA’s Foot-Dragging on Transgenic Salmon, 65 Me. L. Rev. 606 (2013).
- Truth or Consequences?: Commercial Free Speech vs. Public Health Promotion (at the FDA), 21 Health Matrix 31 (2011).
- Coerced Participation in Clinical Trials: Conscripting Human Research Subjects, 62 Admin. L. Rev. 329 (2010).
- Adding Insult to Injury: Paying for Harms Caused by a Competitor’s Copycat Product, 45 Tort Trial & Ins. Prac. L.J. 673 (2010).
- Comfortably Numb: Medicalizing (and Mitigating) Pain-and-Suffering Damages, 42 U. Mich. J.L. Reform 431 (2009).
- This Is Your Products Liability Restatement on Drugs, 74 Brook. L. Rev. 839 (2009).
- Platitudes About “Product Stewardship” in Torts: Continuing Drug Research and Education, 15 Mich. Tel. & Tech. L. Rev. 359 (2009).
- The Little Agency That Could (Act with Indifference to Constitutional and Statutory Strictures), 93 Cornell L. Rev. 901 (2008).
- Too High a Price for Some Drugs?: The FDA Burdens Reproductive Choice, 44 San Diego L. Rev. 231 (2007).
- Treat Yourself: Is Self-Medication the Prescription for What Ails American Health Care?, 19 Harvard J.L. & Tech. 359 (2006).
- Managing Biotechnology’s [R]evolution: Has Guarded Enthusiasm Become Benign Neglect?, 11 Va. J.L. & Tech. 4 (2006).
- An Inventory of Mathematical Blunders in Applying the Loss-of-a-Chance Doctrine, 24 Rev. Litig. 369 (2005).
- Medical Education and Malpractice: What’s the Connection?, 15 Health Matrix 149 (2005).
- Ambivalent Commitments to Federalism in Controlling the Practice of Medicine, 53 U. Kan. L. Rev. 149 (2004).
- A Postmodernist Take on the Human Embryo Research Debate, 36 Conn. L. Rev. 1133 (2004).
- Deputizing Institutional Review Boards to Police (Audit?) Biomedical Research, 25 J. Legal Med. 267 (2004).
- Letter, Trends in Assisted Reproductive Technology, 351 New Eng. J. Med. 398 (2004).
- Assisted Reproductive Technologies and the Pitfalls of Unregulated Biomedical Innovation, 55 Fla. L. Rev. 603 (2003).
- Challenges in the Federal Regulation of Pain Management Technologies, 31 J.L. Med. & Ethics 55 (2003).
- Triage in the Nation’s Medicine Cabinet: The Puzzling Scarcity of Vaccines and Other Drugs, 54 S.C. L. Rev. 741 (2003).
- Letter, Pharmacogenetics, 348 New Eng. J. Med. 2042 (2003).
- The Coming Pharmacogenomics Revolution: Tailoring Drugs to Fit Patients’ Genetic Profiles, 43 Jurimetrics J. 1 (2002).
- Informed Consent and the Elusive Dichotomy Between Standard and Experimental Therapy, 28 Am. J.L. & Med. 361 (2002).
- Medicine’s Epistemology: Mapping the Haphazard Diffusion of Knowledge in the Biomedical Community, 44 Ariz. L. Rev. 373 (2002).
- Letter, Attorney General’s Intrusion into Clinical Practice, 346 New Eng. J. Med. 1918 (2002).
- Letter, Standards for Medical Expert Testimony, 288 JAMA 2971 (2002).
- Civil Jury Nullification, 86 Iowa L. Rev. 1601 (2001).
- A Miscarriage in the Drug Approval Process?: Mifepristone Embroils the FDA in Abortion Politics, 36 Wake Forest L. Rev. 571 (2001).
- Rewarding Regulatory Compliance: The Pursuit of Symmetry in Products Liability, 88 Geo. L.J. 2147 (2000).
- Interpreting Agency Enabling Acts: Misplaced Metaphors in Administrative Law, 41 Wm. & Mary L. Rev. 1463 (2000).
- Scientific “Republicanism”: Expert Peer Review and the Quest for Regulatory Deliberation, 49 Emory L.J. 1033 (2000).
- Divining Regulatory Intent: The Place for a “Legislative History” of Agency Rules, 51 Hastings L.J. 255 (2000).
- What’s Wrong with “Constitutionalizing Food and Drug Law”?, 75 Tul. L. Rev. 137 (2000).
- Peer Review and Regulatory Reform, 30 Envtl. L. Rep. 10,606 (2000).
- Pigeonholing Illness: Medical Diagnosis as a Legal Construct, 50 Hastings L.J. 241 (1999).
- Doubts About Direct Final Rulemaking, 51 Admin. L. Rev. 401 (1999).
- The Executive Line Item Veto and the Judicial Power to Sever: What’s the Difference?, 56 Wash. & Lee L. Rev. 235 (1999).
- Starting from Scratch?: Reinventing the Food Additive Approval Process, 78 B.U. L. Rev. 329 (1998).
- Sanctifying Scientific Peer Review: Publication as a Proxy for Regulatory Decisionmaking, 59 U. Pitt. L. Rev. 677 (1998).
- Authors, Publishers, and Products Liability: Remedies for Defective Information in Books, 77 Or. L. Rev. 1195 (1998).
- Regulating Cigarettes: (Non)sense and Sensibility, 22 S. Ill. U. L.J. 677 (1998).
- Administrative Arm-Twisting in the Shadow of Congressional Delegations of Authority, 1997 Wis. L. Rev. 873 (1997).
- Advertising Prescription Drugs to Consumers: Assessing the Regulatory and Liability Issues, 32 Ga. L. Rev. 141 (1997).
- The FDA’s New Policy on Guidelines: Having Your Cake and Eating It Too, 47 Cath. U. L. Rev. 113 (1997).
- NAFTA’s Impact on the Trade in Pharmaceuticals, 33 Hous. L. Rev. 1293 (1997).
- Reconceptualizing Federal Preemption of Tort Claims as the Government Standards Defense, 37 Wm. & Mary L. Rev. 903 (1996).
- Nicotine Withdrawal: Assessing the FDA’s Effort to Regulate Tobacco Products, 48 Ala. L. Rev. 1 (1996).
- Sham Petitioning as a Threat to the Integrity of the Regulatory Process, 74 N.C. L. Rev. 1 (1995).
- The Imperative to Warn: Disentangling the “Right to Know” from the “Need to Know” About Consumer Product Hazards, 11 Yale J. on Reg. 293 (1994).
- Constraints on the Off-Label Uses of Prescription Drug Products, 16 J. Prods. & Toxics Liab. 139 (1994).
- Amplification of Federal Preemption in Medical Device Cases, 49 Food & Drug L.J. 183 (1994).
- Death of a Salesman: To What Extent Can the FDA Regulate Promotional Statements?, 47 Food & Drug L.J. 309 (1992).
- Note, The Politics of En Banc Review, 102 Harv. L. Rev. 864 (1989).