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Psychedelic Medicine

Law and Policy

Cambridge Bioethics and Law

Burdened with perennially rising costs and responsible for providing health insurance to more than one sixth of all Americans, Medicare in its original form is fiscally and demographically unsustainable. In light of dramatic reforms under the Affordable Care Act (ACA), this book provides a comprehensive overview of the current state of Medicare. Eleanor D. Kinney explains how the ACA addresses systemic problems of cost and volume inflation, quality assurance, and fraud. Recognizing the potential for more radical change in the future, Kinney also explores the potential of Medicare to become a single-payer system. Comparisons are made with national health systems in Canada and the United Kingdom, from which the United States can draw valuable lessons. An approachable yet comprehensive account of Medicare and the ACA, this book will be invaluable for health care professionals and informed citizens.

The Affordable Care Act and Medicare in Comparative Context

Code of Federal Regulations, Title 42 Public Health

A compilation of federal regulations, the CFRs are an authoritative source of government information representing broad subject areas. Title 42 presents regulations that apply to: medical personnel; medical care and examinations; health related grants; fellowships, internships, and training; quarantine, inspection, and licensing; occupational safety and health research; health assessments; vaccines; Medicare and medical assistance programs; and standards and certification of facilities and services. Additions and revisions to this section of the code are posted annually by October. Publication follows within six months.

Code of Federal Regulations, Title 42 Public Health 400-413, 2025

Lexcura Summit

Clinical Intelligence for Attorneys introduces a more disciplined way to interpret medical records, evaluate clinical evidence, and make better-informed litigation decisions.Attorneys routinely receive thousands of pages of medical records, yet the volume of documentation does not guarantee clarity. Important clinical relationships may be buried across multiple facilities, providers, specialties, and episodes of care. A chronology may show what was documented, but it does not necessarily explain what the evidence means, what should have occurred, or whether an alleged failure materially affected the outcome.This book bridges that gap.Michelle Carroll presents Clinical Intelligence as a structured method for examining medical evidence through the combined analysis of record integrity, patient baseline, timeline reconstruction, standard of care, regulatory responsibility, and causation.Written for attorneys handling medical malpractice, personal injury, wrongful death, long-term care, healthcare liability, and other medically complex matters, this book explains how to move beyond surface-level record review and identify the clinical issues that may strengthen, weaken, or fundamentally change a case.Readers will learn how to: Understand the difference between medical documentation and clinical reality.Recognize missing, inconsistent, duplicated, or unreliable records.Establish the patient's true clinical baseline before evaluating injury or deterioration.Identify critical decision points and missed opportunities within the timeline.Distinguish an adverse outcome from a potential breach in the standard of care.Evaluate whether regulatory and organizational failures contributed to the event.Separate clinical correlation from legally meaningful causation.Ask more precise questions of clinicians, experts, witnesses, and opposing counsel.Determine when the evidence supports further investment, early resolution, or strategic withdrawal.Clinical Intelligence does not replace legal judgment, expert testimony, or clinical expertise. It strengthens the attorney's ability to use each of them more effectively.By learning to see the medical record as an interconnected clinical system rather than a collection of documents, attorneys can evaluate cases earlier, prepare more effectively, reduce avoidable assumptions, and make litigation decisions with greater clarity and confidence.

Reconstructing the Patient's Clinical Story before Building the Legal Case

Clinical Intelligence for Attorneys

Before the Cradle to Beyond the Grave

Technology, Health, and Law in Life and Death

This book outlines the role of expert testimony in a trial, including explanations of methods, testing, and science, the legal process, and an overview of the roles of each player. In this, it details the expert witness's role in promoting effective, impactful courtroom testimony.Succeeding as an expert witness requires a basic understanding of who and what experts are and what role they play in rendering their opinions within the courts. The new edition has been fully updated to present key information on the most vital functions the expert plays. This includes the deposition, a discussion of the dangers of false or unsupported testimony, adherence to scientific principles, and the direct and cross-examination testimony of expert witnesses. Each chapter includes key terms, review questions, and thought-provoking discussion questions for further consideration of the topics addressed. Given many recent high-profile cases and increasing incidents of misconduct, this edition focuses heavily on the role of ethics in expert testimony and forensic practice. Outlining established trial-tested tips, forensic scientist Max M. Houck and attorney Christine Funk update renowned lawyer Harold A. Feder's classic book.This is an essential reference for forensic science students entering the work force-in labs and investigative positions-in addition to serving as a crucial resource for more experienced civil, private, and testifying experts in all disciplines.

Successful Expert Testimony

This book constructs a model of informed consent to surgery utilising empirical ethics and socio-legal analysis to bring together medical ethics, medical professional regulation, and medical law. The work includes an original socio-legal analysis of the models of informed consent to surgery present in court judgments and fitness to practise decisions. It constructs such a model using the empirical ethics methodology of reflexive balancing to both develop and challenge its construction. This unified model enables patients to make autonomous choices about surgery by encouraging healthcare professionals to draw upon the patient's subjective perspective, as well as objective viewpoints, when determining what information needs to be given to patients about treatment. It incorporates a focus on the importance of patients understanding that information and having the opportunity to reflect upon it. The outcome is a model of informed consent to surgery that speaks to medical ethics, medical professional regulation, and medical law, giving equivalent weight to the insights offered by each. The book will be an invaluable resource for students, academics and researchers working in the area of Medical Law and Ethics and Bioethics.

A Unified Model

Informed Consent in Medical Ethics, Regulation, and the Law

Mass tort litigation is built on a premise that sounds simple and turns out to be extraordinarily difficult to execute: many people were harmed by the same exposure, in similar ways, and their claims can be pursued together with more efficiency and leverage than any one of them could achieve alone. The premise is sound. The execution is where firms struggle - because "similar" is doing an enormous amount of work in that sentence, and the only way to know whether a given claimant's case is truly similar is to read the medical record with the same rigor a solo practitioner would bring to a single, career-defining case.Most firms cannot do that at scale - not because they lack competence, but because the traditional model of medical record review was never built for the volumes mass tort litigation now produces.Clinical Intelligence for Mass Tort Litigation introduces the discipline that closes that gap. It is not a faster way to summarize medical records, and it is not simply an outsourced review service. It is a structured methodology, built on seven analytical pillars, for determining - claimant by claimant, and across an entire portfolio - what the medical evidence actually supports.Inside, you'll find: <ul><li>The seven-pillar Clinical Intelligence Model: record integrity, baseline profiling, imaging analysis, timeline reconstruction, standard of care review, regulatory and compliance overlay, and causation mapping.</li><li>A tiered review system for applying that model across a portfolio of thousands, so a firm's most expensive resources go only where the evidence says they're needed.</li><li>The economics of Clinical Intelligence, translated into the language firm leadership and litigation funders use.</li><li>Litigation strategy connecting the methodology to bellwether selection, discovery, expert referral, settlement, and defense-vulnerability analysis.</li><li>Operationalizing Clinical Intelligence at enterprise scale, including where artificial intelligence belongs in a clinically governed review process - and where it doesn't.</li><li>Part VIII, From Clinical Finding to Litigation Decision: a dedicated, attorney-facing section, including a mandatory Attorney Decision Matrix, a treatment of general versus specific causation, evidence admissibility under FRE 702/703 and Daubert, and a complete twenty-step worked example following one claimant from intake through final attorney decision.</li><li>Twenty-one appendices, built to be used directly, not read once and set aside.</li><li>Five composite claimant examples, woven throughout the book.</li></ul>Written for attorneys, clinical reviewers, legal nurse consultants, healthcare experts, litigation teams, and claims administrators.Because behind every claimant number is an individual medical story. And that story deserves to be understood before a legal conclusion is reached.

Clinical Intelligence for Mass Tort Litigation

This book argues that patient autonomy and medical negligence make for strange bedfellows. The emphasis on autonomy has distorted orthodox negligence principles, contributing to uncertainty and angst amongst healthcare professionals while eroding trust in the doctor-patient relationship. This work takes the current discourse beyond autonomy - which focuses on the rights of the patient, to agency and shared decision-making - which focus on the relationship between doctor and patient. The core argument is built on a review of the theoretical foundations of negligence and the philosophical conceptions of autonomy. Provocatively, this work argues against a rights-based approach to negligence - which can be confrontational - in favour of a human obligations approach, which is collaborative and thus well suited to the doctor-patient relationship. Drawing on the theoretical analysis, the book identifies doctrinal anomalies in the duty of care, standard of care, causation, and damage. It critically analyses landmark UK Supreme Court cases, including Chester v Afshar, Montgomery v Lanarkshire Health Board, and McCulloch v Forth Valley Health Board, arguing that the law is increasingly detached from the realities of medical practice and reasonable expectations of patients. Primarily based on UK law, the work also discusses Australian, Canadian, and Singaporean law. The book is aimed at the medical and legal fraternities as well as students and scholars of tort law. Doctors and lawyers will gain fresh insights into medical negligence; scholars will find an alternative perspective to orthodoxy with rich material to rethink theory and doctrine in negligence.

Beyond Autonomy

Medical Negligence and the Duty to Advise

Tradd Street Press

"Medical Jurisprudence: A Statement of the Law of Forensic Medicine" is a comprehensive and authoritative examination of the intersection between the legal and medical professions. Written by Elmer D. Brothers, this work serves as a foundational guide to the legal principles governing medical practice and the application of medical science to legal inquiries. The text covers a wide array of critical topics, including the rights and liabilities of physicians, the legal requirements of medical contracts, the nature of professional negligence or malpractice, and the role of the medical expert in judicial proceedings.The book meticulously details the legal framework surrounding patient consent, the confidentiality of medical records, and the complexities of expert testimony. By bridging the gap between clinical knowledge and legal standards, it provides invaluable insights into how medical evidence is interpreted within the courtroom. "Medical Jurisprudence: A Statement of the Law of Forensic Medicine" remains a significant historical reference for legal scholars and medical professionals interested in the evolution of forensic medicine and the enduring principles of medical law. This work offers a clear, structured approach to understanding the duties and protections afforded to practitioners under the law.This work has been selected by scholars as being culturally important, and is part of the knowledge base of civilization as we know it. This work was reproduced from the original artifact, and remains as true to the original work as possible. Therefore, you may see the original copyright references, library stamps (as most of these works have been housed in our most important libraries around the world), and other notations in the work.This work is in the public domain in the United States of America, and possibly other nations. Within the United States, you may freely copy and distribute this work, as no entity (individual or corporate) has a copyright on the body of the work.As a reproduction of a historical artifact, this work may contain missing or blurred pages, poor pictures, errant marks, etc. Scholars believe, and we concur, that this work is important enough to be preserved, reproduced, and made generally available to the public. We appreciate your support of the preservation process, and thank you for being an important part of keeping this knowledge alive and relevant.

A Statement of the Law of Forensic Medicine

Medical Jurisprudence

This book presents a timely overview of how artificial intelligence (AI) is transforming modern healthcare. Combining legal, ethical and practical viewpoints, it explores the impact of AI on patients, clinicians, healthcare organisations and regulators in the EU, UK and US.It delves into the fundamentals of clinical AI systems, explaining how they function and make decisions. It also addresses practical concerns such as safety, fairness, transparency and patient trust. Drawing on real-world examples, such as AI-assisted diagnosis, clinical decision-support tools and machine-learning programmes in hospitals, this book highlights the challenges of aligning law and policy with rapid technological advancements. Key topics explored include bias in medical algorithms, accountability for automation errors and the importance of patient autonomy and data rights for digitally enabled care.The book will appeal to students, policymakers, practitioners and anyone looking to understand the future law of AI in healthcare.

The Law for AI in Healthcare

Towards Social Justice in Dementia Care

Relating to People Living with Dementia as Equals

Psychedelic Medicine

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