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Mills S: Medical Law in Ireland

Medical Law in Ireland

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

Pharmaceutical and medical device manufacturers face relentless and costly waves of product liability claims across U.S. federal and state courts, spanning individual suits, consolidated multidistrict litigation and coordinated proceedings, multi-plaintiff actions, and class actions. As this complex area of litigation continues to expand-often into more treacherous and plaintiff-friendly venues-the stakes for getting strategy right, early and often, have never been higher.

The third edition of Drug and Device Product Liability Litigation Strategy equips litigators with clear, practical guidance from pre-litigation investigations through trial. Reflecting significant developments since the prior edition, it distills the current and evolving legal landscape impacting drug and device lawyers, and offers actionable analysis on the issues that are most likely to influence outcomes: pre-litigation investigation and risk assessment, document preservation and fact discovery, coordination in MDLs and state proceedings, class action challenges, developments in preemption and personal jurisdiction case law, admissibility of expert testimony, dispositive and pre-trial motion practice, jury selection, and trial strategy. 

This edition highlights strategic inflection points and delivers practice-oriented insights to streamline case management and sharpen advocacy. With its emphasis on strategy and results, it is an indispensable resource for lawyers navigating high-profile drug and device litigation in a continually shifting environment.

Drug and Device Product Liability Litigation Strategy

Residential Tenancies

A Cultural History of Nationalism in Europe from 1800 to the Present

Charismatic Nations

This book critically examines the evolving landscape of nanomedicine and its intersection with patent law, focusing on the Indian patent system in comparison with both US and EU frameworks.Through a detailed scientific and legal analysis, this book explores whether nanomedicine inventions meet patentability criteria and examines how current regulations shape innovation in the field. It reveals that nanomedicine innovation, particularly in cancer therapeutics, is often driven by regulatory compliance rather than genuine therapeutic advancements. Empirical research, based on patent claims and prosecution histories from the Indian Patent Office (IPO), the US Patent and Trademark Office (USPTO), and the European Patent Office (EPO), highlights significant gaps in IPO Manuals and guidelines. These inconsistencies have led to the grant of low-quality patents, potentially stifling innovation and undermining India's patent regime. To address these challenges, this book proposes illustrative examples and tests for adequately examining nanomedicine patent claims, aimed at fostering high-quality patents and ensuring robust adjudication of nanomedicine inventions. It uses the IPO as a case study through which important lessons regarding patentability in nanotechnology can be learned.This book will be of interest to researchers in the field of nanotechnology, intellectual property, and patent law.

Innovation in Comparative Context

Nanomedicines in Patent Law

Sexual Offences in Ireland: Practice and Procedure

Provides guidance to the complexities of establishing liability, as well as assistance on running psychiatric claims.

This edition deals with the development of law and practice since the first edition, in particular:
- The Grenfell Tower disaster 
- The change in attitude towards mental health 
- Discussion of Marsh v Ministry of Justice [2017] EWHC 1040 (QB)
- Analysis of cases involving secondary victim claims
- Updates on material contribution 
- Updates on changes to the classification of psychiatric injury 

This title is included in Bloomsbury Professional's Personal Injury Law online service.

Litigating Psychiatric Injury Claims

Hart Studies in Private Law

This ambitious and important book explores the new concept of the doctor-patient relationship, told from the private law perspective. The doctor-patient relationship is different to others. Doctors are required to take positive action when dealing with patients and, accordingly, can be held liable for omissions. However, due to the strict adherence to physical injury as the dominant form of damage in negligence law, a doctor's duty of care is operating, in effect, as a duty not to negligently cause physical injury. This book identifies this to be the main barrier to protecting interests other than bodily integrity in medical negligence law. By so doing, it sets out a new duty of care framework: namely that a doctor would owe a 'positive duty to take care' of the patient's interests. This would ensure that the reasons for requiring doctors to take positive action would be carried through to the damage enquiry. Damage would either not be necessary, or would be expanded to include interests other than bodily integrity. It offers an important and ambitious new way of thinking about the doctor-patient relationship.

A Doctor’s Duty to Take Care

Redefining the Medical Negligence Action

Family Law - Practice and Procedure

Judicial Review

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, Revised as of October 1, 2025

Criminal Law - Sentencing, Procedure and Key Offences

Medical Law in Ireland

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