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The Human Medicines Amendment No 2 Regulations 2014
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Book Synopsis Medicine, patients and the law by : Emma Cave
Download or read book Medicine, patients and the law written by Emma Cave and published by Manchester University Press. This book was released on 2023-06-06 with total page 729 pages. Available in PDF, EPUB and Kindle. Book excerpt: Embryo research, cloning, assisted conception, neonatal care, pandemic vaccine development, saviour siblings, organ transplants, drug trials – modern developments have transformed the field of medicine almost beyond recognition in recent decades and the law struggles to keep up. In this highly acclaimed and very accessible book Margaret Brazier, Emma Cave and Rob Heywood provide an incisive survey of the legal situation in areas as diverse as fertility treatment, patient consent, assisted dying, malpractice and medical privacy. The seventh edition of this book has been fully revised and updated to cover the latest cases, Brexit-related regulatory reform and COVID-19 pandemic measures. Essential reading for healthcare professionals, lecturers, medical and law students, this book is of relevance to all whose perusal of the daily news causes wonder, hope and consternation at the advances and limitations of medicine, patients and the law.
Book Synopsis The Health and Social Care Act 2008 (Regulated Activities) Regulations 2014 by : Great Britain
Download or read book The Health and Social Care Act 2008 (Regulated Activities) Regulations 2014 written by Great Britain and published by . This book was released on 2014-07-11 with total page 32 pages. Available in PDF, EPUB and Kindle. Book excerpt: Enabling power: Health and Social Care Act 2008, ss. 8 (1), 20 (1) to (5A), 35, 86 (2) (4), 87 (1) (2), 161 (3) (4). Issued: 11.07.2014. Made: .- Laid: -. Coming into force: In accord. with reg. 1. Effect: S.I. 2012/921 partially revoked & 2010/781; 2011/2711; 2012/1513 revoked. Territorial extent & classification: E. For approval by resolution of each House of Parliament
Book Synopsis The Drugs Offences Handbook by : Tim Moloney KC
Download or read book The Drugs Offences Handbook written by Tim Moloney KC and published by Bloomsbury Publishing. This book was released on 2018-02-02 with total page 415 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Drugs Offences Handbook provides a comprehensive, focused and concise analysis of the often complex evidential and litigation issues that relate to drugs cases. The law relating to drugs has the broadest span of any specialist area within crime. Evidentially it includes the forensic examination of drugs themselves and evidence linking individuals to drugs, as well as cell site analysis, interrogation of computers and mobile telephones, police powers of search, and the utilisation of police 'expert' witnesses. From a litigation perspective, drugs cases (together with financial crime) make up the vast majority of cases giving rise to money laundering and proceeds of crime issues. In complex supply and importation cases, the financial aspect frequently arises within the evidence as well. Laid out in three broad sections covering Offences, Evidence and Post-conviction, The Drugs Offences Handbook provides expert guidance on key areas such as: - Manufacture and cultivation - Importation - Possession and supply - Police powers of search and seizure - Sentencing and confiscation With reference to all relevant legislation including the Psychoactive Substances Act 2016, the Drugs Act 2005, the Proceeds of Crime Act 2002 as well as analysis of leading cases such as R v Hussain (Shabbir), R v Green and R v Wright, The Drugs Offences Handbook is an essential resource for criminal law practitioners as well as professionals such as drugs agencies, counselling agencies and expert witnesses. Tim Moloney QC, Tom Stevens, Paul Mason, Abigail Bright and Harriet Johnson are all members of Doughty Street Chambers. Steven Bird is the founder and director of Birds Solicitors. The Criminal Practice Series is a series of practical court-style guides covering a number of discrete, specialist areas. They assist users to identify cases, rules and regulations relevant to the specific topic quickly and easily. For more information please visit www.bloomsburyprofessional.com/criminal
Book Synopsis Dimond's Legal Aspects of Nursing by : Richard Griffith
Download or read book Dimond's Legal Aspects of Nursing written by Richard Griffith and published by Pearson UK. This book was released on 2019 with total page 1193 pages. Available in PDF, EPUB and Kindle. Book excerpt: Written specifically for student nurses as well as those already in practice, Dimond's Legal Aspects of Nursing is your essential practical guide to the legal principles you need to be aware of in your everyday nursing practice. Building on previous editions of the book by Bridgit Dimond, this 8th edition has been significantly reworked by a new author team with extensive experience in teaching nursing law. It has also been fully updated and revised in line with recent legal developments and the new Nursing standards to ensure it continues to meet the requirements of nursing law modules.
Book Synopsis The Textbook of Non-Medical Prescribing by : Dilyse Nuttall
Download or read book The Textbook of Non-Medical Prescribing written by Dilyse Nuttall and published by John Wiley & Sons. This book was released on 2019-08-28 with total page 374 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Textbook of Non-Medical Prescribing is an authoritative and accessible overview of the vital skills, contemporary issues and essential knowledge relevant to both students and healthcare practitioners. Written as a response to the growing emphasis placed on prescribing in the modern health service, this text provides up-to-date information on safe and effective prescribing. This wide-ranging book helps students and trainees develop foundational knowledge of the key areas and prescribing competencies and provides healthcare professionals with a continued source of current information. Now in its third edition, this text has been fully updated and revised to reflect changes in legislation, current practices and new guidelines. New and updated topics include independent prescribing for therapeutic radiologists, supplementary prescribing for dietitians, paramedics working in advanced roles to independently prescribe and the Royal Pharmaceutical Society's Competency Framework for all Prescribers. Provides up-to-date information essential to safe and effective prescribing in a clear, easy-to-understand style Discusses current issues and practices in pharmacology, prescribing and therapeutics and medicine management Links to the Royal Pharmaceutical Society's Competency Framework for all Prescribers for non-medical prescribers Presents learning objectives, key theme summaries, activities and numerous case studies Offers access to additional online resources including interactive exercises, quizzes, self-assessment tests and web links The Textbook of Non-Medical Prescribing is an essential resource for students, nurses, dieticians, pharmacists, and allied health practitioners pursuing a prescribing qualification or looking for an updated refresher on the subject.
Book Synopsis Mayes' Midwifery - E-Book by : Sue Macdonald
Download or read book Mayes' Midwifery - E-Book written by Sue Macdonald and published by Elsevier Health Sciences. This book was released on 2023-05-23 with total page 1534 pages. Available in PDF, EPUB and Kindle. Book excerpt: Mayes' Midwifery is a core text for students in the UK, known and loved for its in-depth approach and its close alignment with curricula and practice in this country. The sixteenth edition has been fully updated by leading midwifery educators Sue Macdonald and Gail Johnson, and input from several new expert contributors ensures this book remains at the cutting edge. The text covers all the main aspects of midwifery in detail, including the various stages of pregnancy, possible complexities around childbirth, and psychological and social considerations related to women's health. It provides the most recent evidence along with detailed anatomy and physiology information, and how these translate into practice. Packed full of case studies, reflective activities and images, and accompanied by an ancillary website with 600 multiple choice questions and downloadable images, Mayes' Midwifery makes learning easy for nursing students entering the profession as well as midwives returning to practice and qualified midwives working in different settings in the UK and overseas. - Expert contributors include midwifery academics and clinicians, researchers, physiotherapists, neonatal nurse specialists, social scientists and legal experts - Learning outcomes and key points to support structured study - Reflective activities to apply theory to practice - Figures, tables and breakout boxes help navigation and revision - Associated online resources with over 600 MCQs, reflective activities, case studies, downloadable image bank to help with essay and assignment preparation - Further reading to deepen knowledge and understanding - New chapters addressing the issues around being a student midwife and entering the profession - More detail about FGM and its legal implications, as well as transgender/binary individuals in pregnancy and childbirth - New information on infection and control following from the COVID-19 pandemic - Enhanced artwork program
Book Synopsis Clinical Negligence by : Dr Michael Powers KC
Download or read book Clinical Negligence written by Dr Michael Powers KC and published by Bloomsbury Publishing. This book was released on 2023-07-31 with total page 1609 pages. Available in PDF, EPUB and Kindle. Book excerpt: "I would highly recommend this book...It is high quality, clear and comprehensive and will no doubt prove an invaluable source of reference. Five stars on all counts." Tim Kevan, co-editor, PIBULJ.COM This book remains the only text of its kind to cover both the medical and legal aspects of medical negligence. Written by a team of more than 60 experts, it continues to provide the most comprehensive and authoritative guidance on all aspects of clinical negligence claims, from bringing an action for damages to presenting expert evidence in court. It also includes detailed consideration of funding and cost implications. Those needing clear guidance to make the best possible preparations for an action will find all they need here. The new 6th edition has been fully revised and restructured, including new chapters on the future of clinical negligence litigation, cardiology, gynaecology, obstetrics, haematology , and also includes coverage and analysis of recent key cases such as: - Williams v Bermuda Hospitals [2016] UKPC 4 (causation) - R (on the application of Maughan) v HM Senior Coroner for Oxfordshire [2020] UKSC 46 (suicide in inquests) - Darnley v Croydon Health Authority [2018] UKSC 50 (duty of care owed by receptionist) - ABC v St George's Hosp [2020] EWHC 455 (Huntington's chorea confidentiality) - Swift v Carpenter [2020] EWCA Civ 1295 (future accommodation costs) - Whittington Hospital NHS Trust v XX [2020] UKSC 14 (damages for surrogacy) - Khan v Meadows [2021] UKSC 21 (scope of duty of care) - Nguyen v HM Assistant Coroner for Inner West London [2021] EWHC 3354 (sufficiency of inquiry) Easy-to-access structure The new edition maintains its easy-to-access, two-part structure. The first part, set out in 16 chapters, deals with legal aspects of medical malpractice, including complaints procedures, poor performance and medical professional governance, preparation of medical evidence, settlements and trial. There are also chapters on product liability, and coronial law. The final 27 chapters in the second part cover the risks associated with particular areas of specialist medical practice. This title is included in Bloomsbury Professional's Clinical Negligence online service.
Book Synopsis Mason and McCall Smith's Law and Medical Ethics by : Graeme T. Laurie
Download or read book Mason and McCall Smith's Law and Medical Ethics written by Graeme T. Laurie and published by Oxford University Press. This book was released on 2016 with total page 795 pages. Available in PDF, EPUB and Kindle. Book excerpt: This classic textbook has provided students of medical law and ethics with a framework for exploring this fascinating subject for over 30 years. This book provides extensive coverage and insight into recent judicial decisions and statutory developments across the United Kingdom alongside the authors' own opinion on current debates and controversies to help you to formulate your own views and arguments. The tenth edition has evolved to reflect changes in the law and shifting ethical opinions. In setting the UK context, it continues to take a comparative approach, including reference to the Scottish position where relevant. A specific chapter on the European dimension in health care and the particular importance attached to this shift in influence from transatlantic jurisdictions to those of the EU is included. Mason & McCall Smith's Law & Medical Ethics is essential reading for any serious medical law student or practitioner. Book jacket.
Download or read book Medical Law written by Jo Samanta and published by Bloomsbury Publishing. This book was released on 2015-05-28 with total page 631 pages. Available in PDF, EPUB and Kindle. Book excerpt: The second edition of a major text provides a thorough exploration of medical law and ethics, written from the perspective of authors who are medical and health care practitioners as well as law lecturers. This unique combination of academic knowledge and professional experience provides a unique perspective through which the subject is examined with academic rigour underpinned by practical insights. The text features an innovative series of scenarios threaded through each chapter to illustrate the practical realities behind the rules and concepts discussed. The format also includes mind maps, key terms, end of chapter summaries, self-test exercises and suggestions for further reading.
Book Synopsis The Law of Off-label Uses of Medicines by : Andrea Parziale
Download or read book The Law of Off-label Uses of Medicines written by Andrea Parziale and published by Taylor & Francis. This book was released on 2022-08-12 with total page 183 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book examines the regulatory framework for untested and unapproved uses (off-label uses) of medicines in the EU, UK, and USA. Before reaching patients, medicines are extensively tested by manufacturers and approved by regulators to minimise the risk of adverse reactions. However, physicians can prescribe pharmaceuticals for off-label uses, widespread in paediatrics, oncology, rare diseases and, more recently, in treatment for Covid-19. While off-label uses may offer hope, they may also expose patients to risks and uncertainties. Clarification is therefore needed to improve the protection of patients' rights while enhancing legal certainty for health actors. To this end, this work clarifies the regulatory mechanisms and litigation trends concerning off-licence prescriptions in these jurisdictions. It assesses how traditional, prevention-driven regulatory and civil liability rules are being adapted to tackle potential risks and scientific uncertainty. The book outlines the applicable regulations, as well as considering Brexit’s impact on off-label policies in the UK, and EU and national off-label policies in the context of the fight against the Covid-19 pandemic. It also explores under what conditions physicians, manufacturers, or regulators must compensate patients injured by untested prescriptions. The book will be an essential resource for researchers, academics and policy-makers working in the areas of medical law and ethics, public health law, pharmaceutical law and private comparative law.
Author :National Academies of Sciences, Engineering, and Medicine Publisher :National Academies Press ISBN 13 :0309468086 Total Pages :235 pages Book Rating :4.3/5 (94 download)
Book Synopsis Making Medicines Affordable by : National Academies of Sciences, Engineering, and Medicine
Download or read book Making Medicines Affordable written by National Academies of Sciences, Engineering, and Medicine and published by National Academies Press. This book was released on 2018-03-01 with total page 235 pages. Available in PDF, EPUB and Kindle. Book excerpt: Thanks to remarkable advances in modern health care attributable to science, engineering, and medicine, it is now possible to cure or manage illnesses that were long deemed untreatable. At the same time, however, the United States is facing the vexing challenge of a seemingly uncontrolled rise in the cost of health care. Total medical expenditures are rapidly approaching 20 percent of the gross domestic product and are crowding out other priorities of national importance. The use of increasingly expensive prescription drugs is a significant part of this problem, making the cost of biopharmaceuticals a serious national concern with broad political implications. Especially with the highly visible and very large price increases for prescription drugs that have occurred in recent years, finding a way to make prescription medicinesâ€"and health care at largeâ€"more affordable for everyone has become a socioeconomic imperative. Affordability is a complex function of factors, including not just the prices of the drugs themselves, but also the details of an individual's insurance coverage and the number of medical conditions that an individual or family confronts. Therefore, any solution to the affordability issue will require considering all of these factors together. The current high and increasing costs of prescription drugsâ€"coupled with the broader trends in overall health care costsâ€"is unsustainable to society as a whole. Making Medicines Affordable examines patient access to affordable and effective therapies, with emphasis on drug pricing, inflation in the cost of drugs, and insurance design. This report explores structural and policy factors influencing drug pricing, drug access programs, the emerging role of comparative effectiveness assessments in payment policies, changing finances of medical practice with regard to drug costs and reimbursement, and measures to prevent drug shortages and foster continued innovation in drug development. It makes recommendations for policy actions that could address drug price trends, improve patient access to affordable and effective treatments, and encourage innovations that address significant needs in health care.
Book Synopsis Psychiatric Intensive Care by : Roland Dix
Download or read book Psychiatric Intensive Care written by Roland Dix and published by Cambridge University Press. This book was released on 2024-03-31 with total page 359 pages. Available in PDF, EPUB and Kindle. Book excerpt: The new edition of this practical textbook provides guidance on managing severely ill psychiatric patients in secure hospital settings.
Author : Publisher :Oxford University Press ISBN 13 :0198898606 Total Pages :1264 pages Book Rating :4.1/5 (988 download)
Download or read book written by and published by Oxford University Press. This book was released on with total page 1264 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Clinical Pharmacy and Therapeutics E-Book by : Cate Whittlesea
Download or read book Clinical Pharmacy and Therapeutics E-Book written by Cate Whittlesea and published by Elsevier Health Sciences. This book was released on 2018-09-11 with total page 1112 pages. Available in PDF, EPUB and Kindle. Book excerpt: 'This new edition of Clinical Pharmacy and Therapeutics was really very helpful when I was doing an MSc course in Advancing Pharmacy Practice and it was really very helpful in all the clinical diseases I have to read for my PBL. I also used it as one of my most reliable reference books for the in-course simulation ward rounds and other clinical case studies. It is a great book to have as a practising clinical or hospital pharmacist or even community pharmacist. It will also be of great use to anyone doing a course in pharmacotherapy. This book will always be of use to you throughout your studentship or when practising after graduation. It is also more portable than most other pharmacotherapy textbooks with the same amount of information.' Now in its sixth edition, this best-selling, multi-disciplinary textbook continues to draw on the skills of pharmacists, clinicians and nurses to present optimal drug regimens. The authors integrate an understanding of the disease processes with an appreciation of the pathophysiological processes, clinical pharmacy and the evidence base. Each chapter is co-written by a pharmacist and a clinician, and each chapter begins with key points and ends with cases to test understanding. The sixth edition is now on StudentConsult for the first time, giving online access to the full text. - Key points boxes at the beginning of each chapter - Case-study boxes throughout the chapters - Each chapter co-written by a pharmacist and a clinician - In-depth treatment of therapeutics to support pharmaceutical prescribing - Logical order and format: key points, epidemiology, aetiology, disease, clinical manifestations, investigations and treatment, drugs used in treatment. - Dosage reference sources given where appropriate, along with useful websites and further reading for each chapter. - New co-editor, Karen Hodson - Over 10 new authors - Now in 4-colour - On StudentConsult for the first time - New chapter on Dementia - Many new and revised illustrations - Chapters revised to include advances in therapeutics and changes to dose regimens and licensed indications - Updated case studies
Book Synopsis Intellectual Property Rights in Pharmaceutical Test Data by : Adam Buick
Download or read book Intellectual Property Rights in Pharmaceutical Test Data written by Adam Buick and published by Springer Nature. This book was released on 2023-05-12 with total page 236 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book considers the intellectual property protection of clinical test data that has been submitted to governments, in particular through test data exclusivity rights. It focuses on how these intellectual property rights first emerged in the early 1980s, how they have globalised over the past four decades, and what impact they have had upon access to medicine. This book makes a number of significant and original contributions to the literature around the protection of submitted test data. First, the book draws upon the theory of regulatory globalisation to provide an explanation of how intellectual property rights in submitted pharmaceutical test data have become nearly ubiquitous in the legal systems of most major economies. Second, through a comprehensive analysis and synthesis of provisions on the protection of submitted test data in free trade agreements, as well as a comparison of a range of national approaches to the protection of submitted test data, it reveals the broader global regulatory pattern that has given rise to these intellectual property rights. Third, by analysing data on drug approvals in the US, it provides an empirical insight into the impact of test data exclusivity in national pharmaceutical markets. Fourth, the book covers a number of developments regarding test data exclusivity that have occurred as a result of responses to the COVID-19 pandemic, both at the national level as well as at the World Trade Organisation (WTO). This book will appeal to academics researching the intersection of intellectual property and the life sciences, civil society activists working to promote access to medicines, and students (particularly those at the post-graduate level) studying the relationship between intellectual property and medicine.
Author :National Academies of Sciences, Engineering, and Medicine Publisher :National Academies Press ISBN 13 :0309459575 Total Pages :483 pages Book Rating :4.3/5 (94 download)
Book Synopsis Pain Management and the Opioid Epidemic by : National Academies of Sciences, Engineering, and Medicine
Download or read book Pain Management and the Opioid Epidemic written by National Academies of Sciences, Engineering, and Medicine and published by National Academies Press. This book was released on 2017-09-28 with total page 483 pages. Available in PDF, EPUB and Kindle. Book excerpt: Drug overdose, driven largely by overdose related to the use of opioids, is now the leading cause of unintentional injury death in the United States. The ongoing opioid crisis lies at the intersection of two public health challenges: reducing the burden of suffering from pain and containing the rising toll of the harms that can arise from the use of opioid medications. Chronic pain and opioid use disorder both represent complex human conditions affecting millions of Americans and causing untold disability and loss of function. In the context of the growing opioid problem, the U.S. Food and Drug Administration (FDA) launched an Opioids Action Plan in early 2016. As part of this plan, the FDA asked the National Academies of Sciences, Engineering, and Medicine to convene a committee to update the state of the science on pain research, care, and education and to identify actions the FDA and others can take to respond to the opioid epidemic, with a particular focus on informing FDA's development of a formal method for incorporating individual and societal considerations into its risk-benefit framework for opioid approval and monitoring.
Book Synopsis Medicines (Advertising) Regulations 1994 by : Great Britain
Download or read book Medicines (Advertising) Regulations 1994 written by Great Britain and published by . This book was released on 1994 with total page 20 pages. Available in PDF, EPUB and Kindle. Book excerpt: Medicines (Advertising) Regulations 1994
