Unhealthy Pharmaceutical Regulation
DOWNLOAD
FREE 30 Days
Download Unhealthy Pharmaceutical Regulation PDF/ePub or read online books in Mobi eBooks. Click Download or Read Online button to get Unhealthy Pharmaceutical Regulation book now. This website allows unlimited access to, at the time of writing, more than 1.5 million titles, including hundreds of thousands of titles in various foreign languages. If the content not found or just blank you must refresh this page
Unhealthy Pharmaceutical Regulation
DOWNLOAD
FREE 30 Days
Author : C. Davis
language : en
Publisher: Springer
Release Date : 2013-11-08
Unhealthy Pharmaceutical Regulation written by C. Davis and has been published by Springer this book supported file pdf, txt, epub, kindle and other format this book has been release on 2013-11-08 with Medical categories.
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.
Bad Pharma
DOWNLOAD
FREE 30 Days
Author : Ben Goldacre
language : en
Publisher: Farrar, Straus and Giroux
Release Date : 2013-02-05
Bad Pharma written by Ben Goldacre and has been published by Farrar, Straus and Giroux this book supported file pdf, txt, epub, kindle and other format this book has been release on 2013-02-05 with Science categories.
We like to imagine that medicine is based on evidence and the results of fair testing and clinical trials. In reality, those tests and trials are often profoundly flawed. We like to imagine that doctors who write prescriptions for everything from antidepressants to cancer drugs to heart medication are familiar with the research literature about a drug, when in reality much of the research is hidden from them by drug companies. We like to imagine that doctors are impartially educated, when in reality much of their education is funded by the pharmaceutical industry. We like to imagine that regulators have some code of ethics and let only effective drugs onto the market, when in reality they approve useless drugs, with data on side effects casually withheld from doctors and patients. All these problems have been shielded from public scrutiny because they're too complex to capture in a sound bite. But Ben Goldacre shows that the true scale of this murderous disaster fully reveals itself only when the details are untangled. He believes we should all be able to understand precisely how data manipulation works and how research misconduct in the medical industry affects us on a global scale. With Goldacre's characteristic flair and a forensic attention to detail, Bad Pharma reveals a shockingly broken system and calls for regulation. This is the pharmaceutical industry as it has never been seen before.
The Interplay Of Global Standards And Eu Pharmaceutical Regulation
DOWNLOAD
FREE 30 Days
Author : Sabrina Roettger-Wirtz
language : en
Publisher:
Release Date : 2021
The Interplay Of Global Standards And Eu Pharmaceutical Regulation written by Sabrina Roettger-Wirtz and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2021 with Drugs categories.
"This book analyses the implementation of global pharmaceutical impact standards in the European risk regulation framework for pharmaceuticals and questions its legitimacy. Global standards increasingly shape the risk regulation law and policy in the European Union and the area of pharmaceuticals is no exception to this tendency. As this book shows, global pharmaceutical standards set by the International Council for Harmonisation of Technical Requirements for the Registration of Pharmaceuticals for Human Use (ICH), after they are adopted through the European Medicines Agency (EMA), are an important feature of the regulatory framework for pharmaceuticals in the EU. In addition to analysing the influence of these global standards in the EU legal and policy framework, the book questions the legitimacy of the Union's reliance on global standards in terms of core administrative law principles of participation, transparency and independence of expertise. It also critically examines the accountability of the European Commission and the European Medicines Agency as participants in the global standard-setting and main implementation gateway of the global pharmaceutical standards into the European Union."--
Pharmaceutical Regulation In Europe
DOWNLOAD
FREE 30 Days
Author : Panos Kanavos
language : en
Publisher:
Release Date : 2002
Pharmaceutical Regulation In Europe written by Panos Kanavos and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2002 with Drugs categories.
Pharmaceutical Regulation In Europe
DOWNLOAD
FREE 30 Days
Author : Panos Kanavos
language : en
Publisher:
Release Date : 2000-05-01
Pharmaceutical Regulation In Europe written by Panos Kanavos and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2000-05-01 with Medical categories.
Pharmaceutical And Medical Device Safety
DOWNLOAD
FREE 30 Days
Author : Sonia Macleod
language : en
Publisher:
Release Date : 2019
Pharmaceutical And Medical Device Safety written by Sonia Macleod and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2019 with categories.
"This book examines how regulatory and liability mechanisms have impacted upon product safety decisions in the pharmaceutical and medical devices sectors in Europe, the USA and beyond since the 1950s. Thirty-five case studies illustrate the interplay between the regulatory regimes and litigation. Observations from medical practice have been the overwhelming means of identifying post-marketing safety issues. Drug and device safety decisions have increasingly been taken by public regulators and companies within the framework of the comprehensive regulatory structure that has developed since the 1960s. In general, product liability cases have not identified or defined safety issues, and function merely as compensation mechanisms. This is unsurprising as the thresholds for these two systems differ considerably; regulatory action can be triggered by the possibility that a product might be harmful, whereas establishing liability in litigation requires proving that the product was actually harmful. As litigation normally post-dates regulatory implementation, the 'private enforcement' of public law has generally not occurred in these sectors. This has profound implications for the design of sectoral regulatory and liability regimes, including associated features such as extended liability law, class actions and contingency fees. This book forms a major contribution to the academic debate on the comparative utility of regulatory and liability systems, on public versus private enforcement, and on mechanisms of behaviour control."--Bloomsbury Publishing.
Transparency Power And Influence In The Pharmaceutical Industry
DOWNLOAD
FREE 30 Days
Author : Katherine Fierlbeck
language : en
Publisher: University of Toronto Press
Release Date : 2021
Transparency Power And Influence In The Pharmaceutical Industry written by Katherine Fierlbeck and has been published by University of Toronto Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2021 with Pharmaceutical policy categories.
Transparency, Power, and Influence in the Pharmaceutical Industry evaluates the progress made in holding the pharmaceutical industry to account through greater transparency.
Pharmaceutical Freedom
DOWNLOAD
FREE 30 Days
Author : Jessica Flanigan
language : en
Publisher: Oxford University Press
Release Date : 2017
Pharmaceutical Freedom written by Jessica Flanigan and has been published by Oxford University Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2017 with Law categories.
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.--
Unhealthy Politics
DOWNLOAD
FREE 30 Days
Author : Eric M. Patashnik
language : en
Publisher: Princeton University Press
Release Date : 2020-07-21
Unhealthy Politics written by Eric M. Patashnik and has been published by Princeton University Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2020-07-21 with Political Science categories.
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.
The Influence Of The Pharmaceutical Industry
DOWNLOAD
FREE 30 Days
Author : Great Britain: Parliament: House of Commons: Health Committee
language : en
Publisher: The Stationery Office
Release Date : 2005-04-26
The Influence Of The Pharmaceutical Industry written by Great Britain: Parliament: House of Commons: Health Committee and has been published by The Stationery Office this book supported file pdf, txt, epub, kindle and other format this book has been release on 2005-04-26 with Political Science categories.
Incorporating HC 1030-i to iii.