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Section 1557 is the nondiscrimination provision of the Affordable Care Act (ACA). This brief guide explains Section 1557 in more detail and what your practice needs to do to meet the requirements of this federal law. Includes sample notices of nondiscrimination, as well as taglines translated for the top 15 languages by state.
Written in an engaging and accessible style, this book is a must-read for anyone interested in the intersection of law and medicine. Don't miss out on this invaluable resource-order your copy today! In addition you are entitled to get free online advice from Dr. Binoy Gupta (email:- [email protected]) on any issue relating to Medical Negligence For the Medical Professional This book will help you understand: 1. What is Medical Negligence 2. What precaution the Doctor should take to avoid being involved in litigation. 3. What records the Doctor should maintain.
Given how frequently the pharmacy and healthcare industries evolve, it's critical to comprehend the laws and regulations that govern the sector. This book aims to provide a comprehensive overview of the intricate network of Indian laws, statutes, and regulations that control the practice of pharmacy. The discipline of pharmacy is governed by an extensive set of laws, guidelines, and moral principles that are essential to safeguarding the public's health and guaranteeing the responsible, efficient, and safe practice of the profession. These rules, laws, and principles are fundamental to the pharmacy industry. Each section delves deeply into the intricate legal framework that oversees the pharmacy sector, covering everything from the fundamental guidelines provided by the Pharmacy Act of 1948 to the particulars of manufacturing, marketing, and shipping medications as outlined by the Drugs and Cosmetics Act of 1940. The book gives readers a tour of regulatory organisations, demonstrating their functions and methods, such as the National Pharmaceutical Pricing Authority and the Pharmacy Council of India. Students will gain knowledge of the legal definitions and classifications of pharmaceuticals and medications, as well as the responsibilities and duties of chemists and the ethical dilemmas that arise in the practice of their profession. This book provides a thorough grasp of the moral and legal principles that underpin the pharmaceutical industry. It addresses a wide range of topics, such as drug production and distribution, consumer protection, and clinical research.
Derived from the renowned multi-volume International Encyclopaedia of Laws, this convenient volume provides comprehensive analysis of the law affecting the physician-patient relationship in India. Cutting across the traditional compartments with which lawyers are familiar, medical law is concerned with issues arising from this relationship, and not with the many wider juridical relations involved in the broader field of health care law. After a general introduction, the book systematically describes law related to the medical profession, proceeding from training, licensing, and other aspects of access to the profession, through disciplinary and professional liability and medical ethics considerations and quality assurance, to such aspects of the physician-patient relationship as rights and duties of physicians and patients, consent, privacy, and access to medical records. Also covered are specific issues such as organ transplants, human medical research, abortion, and euthanasia, as well as matters dealing with the physician in relation to other health care providers, health care insurance, and the health care system. Succinct and practical, this book will prove to be of great value to professional organizations of physicians, nurses, hospitals, and relevant government agencies. Lawyers representing parties with interests in India will welcome this very useful guide, and academics and researchers will appreciate its comparative value as a contribution to the study of medical law in the international context.
There are significant variations in how healthcare systems and health professionals are regulated globally. One feature that they increasingly have in common is an emphasis on the value of including members of the public in quality assurance processes. While many argue that this will help better serve the public interest, others question how far the changing regulatory reform agenda is still dominated by medical interests. Bringing together leading academics worldwide, this collection compares and critically examines the ways in which different countries are regulating healthcare in general, and health professions in particular, in the interest of users and the wider public. It is the first book in the Sociology of Health Professions series.
This volume, developed by the Observatory together with OECD, provides an overall conceptual framework for understanding and applying strategies aimed at improving quality of care. Crucially, it summarizes available evidence on different quality strategies and provides recommendations for their implementation. This book is intended to help policy-makers to understand concepts of quality and to support them to evaluate single strategies and combinations of strategies.