Unhealthy Pharmaceutical Regulation PDF Download
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Author | : C. Davis |
Publisher | : Springer |
Total Pages | : 333 |
Release | : 2013-11-08 |
Genre | : Medical |
ISBN | : 1137349476 |
Download Unhealthy Pharmaceutical Regulation Book in PDF, ePub and Kindle
This is the first book to examine how effectively American and supranational EU governments have regulated innovative pharmaceuticals during the last 30 years regarding public health. It explains why pharmaceutical regulation has been misdirected by commercial interests and misconceived ideologies.
Author | : Ben Goldacre |
Publisher | : Macmillan |
Total Pages | : 479 |
Release | : 2014-04 |
Genre | : Business & Economics |
ISBN | : 0865478066 |
Download Bad Pharma Book in PDF, ePub and Kindle
Originally published in 2012, revised edition published in 2013, by Fourth Estate, Great Britain; Published in the United States in 2012, revised edition also, by Faber and Faber, Inc.
Author | : Katherine Fierlbeck |
Publisher | : University of Toronto Press |
Total Pages | : 303 |
Release | : 2021 |
Genre | : Pharmaceutical policy |
ISBN | : 148752904X |
Download Transparency, Power, and Influence in the Pharmaceutical Industry Book in PDF, ePub and Kindle
Transparency, Power, and Influence in the Pharmaceutical Industry evaluates the progress made in holding the pharmaceutical industry to account through greater transparency.
Author | : Institute of Medicine |
Publisher | : National Academies Press |
Total Pages | : 377 |
Release | : 2013-06-20 |
Genre | : Medical |
ISBN | : 0309269393 |
Download Countering the Problem of Falsified and Substandard Drugs Book in PDF, ePub and Kindle
The adulteration and fraudulent manufacture of medicines is an old problem, vastly aggravated by modern manufacturing and trade. In the last decade, impotent antimicrobial drugs have compromised the treatment of many deadly diseases in poor countries. More recently, negligent production at a Massachusetts compounding pharmacy sickened hundreds of Americans. While the national drugs regulatory authority (hereafter, the regulatory authority) is responsible for the safety of a country's drug supply, no single country can entirely guarantee this today. The once common use of the term counterfeit to describe any drug that is not what it claims to be is at the heart of the argument. In a narrow, legal sense a counterfeit drug is one that infringes on a registered trademark. The lay meaning is much broader, including any drug made with intentional deceit. Some generic drug companies and civil society groups object to calling bad medicines counterfeit, seeing it as the deliberate conflation of public health and intellectual property concerns. Countering the Problem of Falsified and Substandard Drugs accepts the narrow meaning of counterfeit, and, because the nuances of trademark infringement must be dealt with by courts, case by case, the report does not discuss the problem of counterfeit medicines.
Author | : Jessica Flanigan |
Publisher | : Oxford University Press |
Total Pages | : 289 |
Release | : 2017 |
Genre | : Law |
ISBN | : 0190684542 |
Download Pharmaceutical Freedom Book in PDF, ePub and Kindle
Jessica Flanigan defends patients' rights of self-medication on the grounds that same moral reasons against medical paternalism in clinical contexts are also reasons against paternalistic pharmaceutical policies, including prohibitive approval processes and prescription requirements.
Author | : Markus Müller |
Publisher | : Springer Science & Business Media |
Total Pages | : 438 |
Release | : 2011-02-04 |
Genre | : Medical |
ISBN | : 3709101441 |
Download Clinical Pharmacology: Current Topics and Case Studies Book in PDF, ePub and Kindle
Today we witness an eventful time in which the powerful new forces of genomics, information technology and economics are rapidly changing the science and art of medicine. This will require more specialization than ever before. However, there is also an increasing demand for an integrated approach, which is provided by the discipline of Clinical Pharmacology (CP). CP pursues a scientific goal by studying drug action in patients and volunteers, a clinical goal by administering appropriate drug therapy and a regulatory goal by assessing the risk/benefit ratio of drug candidates in drug development and reimbursement. This introduction to current topics of CP covers traditional topics of clinical drug research and trial methodology but also provides insight in current topics like genomics, imaging technology and issues in drug reimbursement. A number of concrete case studies in clinical drug research and development help to give a better understanding of the general principles of CP.
Author | : Institute of Medicine |
Publisher | : National Academies Press |
Total Pages | : 322 |
Release | : 1996-04-25 |
Genre | : Medical |
ISBN | : 0309053862 |
Download Radiation in Medicine Book in PDF, ePub and Kindle
Does radiation medicine need more regulation or simply better-coordinated regulation? This book addresses this and other questions of critical importance to public health and safety. The issues involved are high on the nation's agenda: the impact of radiation on public safety, the balance between federal and state authority, and the cost-benefit ratio of regulation. Although incidents of misadministration are rare, a case in Pennsylvania resulting in the death of a patient and the inadvertent exposure of others to a high dose of radiation drew attention to issues concerning the regulation of ionizing radiation in medicine and the need to examine current regulatory practices. Written at the request from the Nuclear Regulatory Commission (NRC), Radiation in Medicine reviews the regulation of ionizing radiation in medicine, focusing on the NRC's Medical Use Program, which governs the use of reactor-generated byproduct materials. The committee recommends immediate action on enforcement and provides longer term proposals for reform of the regulatory system. The volume covers: Sources of radiation and their use in medicine. Levels of risk to patients, workers, and the public. Current roles of the Nuclear Regulatory Commission, other federal agencies, and states. Criticisms from the regulated community. The committee explores alternative regulatory structures for radiation medicine and explains the rationale for the option it recommends in this volume. Based on extensive research, input from the regulated community, and the collaborative efforts of experts from a range of disciplines, Radiation in Medicine will be an important resource for federal and state policymakers and regulators, health professionals involved in radiation treatment, developers and producers of radiation equipment, insurance providers, and concerned laypersons.
Author | : Eric M. Patashnik |
Publisher | : Princeton University Press |
Total Pages | : 283 |
Release | : 2020-07-21 |
Genre | : Political Science |
ISBN | : 0691208565 |
Download Unhealthy Politics Book in PDF, ePub and Kindle
How partisanship, polarization, and medical authority stand in the way of evidence-based medicine The U.S. medical system is touted as the most advanced in the world, yet many common treatments are not based on sound science. Unhealthy Politics sheds new light on why the government's response to this troubling situation has been so inadequate, and why efforts to improve the evidence base of U.S. medicine continue to cause so much political controversy. This critically important book paints a portrait of a medical industry with vast influence over which procedures and treatments get adopted, and a public burdened by the rising costs of health care yet fearful of going against "doctor's orders." Now with a new preface by the authors, Unhealthy Politics offers vital insights into the limits of science, expertise, and professionalism in American politics.
Author | : Divya Vohora |
Publisher | : Academic Press |
Total Pages | : 527 |
Release | : 2017-11-14 |
Genre | : Medical |
ISBN | : 0128020989 |
Download Pharmaceutical Medicine and Translational Clinical Research Book in PDF, ePub and Kindle
Pharmaceutical Medicine and Translational Clinical Research covers clinical testing of medicines and the translation of pharmaceutical drug research into new medicines, also focusing on the need to understand the safety profile of medicine and the benefit-risk balance. Pharmacoeconomics and the social impact of healthcare on patients and public health are also featured. It is written in a clear and straightforward manner to enable rapid review and assimilation of complex information and contains reader-friendly features.As a greater understanding of these aspects is critical for students in the areas of pharmaceutical medicine, clinical research, pharmacology and pharmacy, as well as professionals working in the pharmaceutical industry, this book is an ideal resource. Includes detailed coverage of current trends and key topics in pharmaceutical medicine, including biosimilars, biobetters, super generics, and Provides a comprehensive look at current and important aspects of the science and regulation of drug and biologics discovery
Author | : Upton Sinclair |
Publisher | : |
Total Pages | : 442 |
Release | : 1920 |
Genre | : Chicago (Ill.) |
ISBN | : |
Download The Jungle Book in PDF, ePub and Kindle