Generisk
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Generisk
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Author :
language : en
Publisher:
Release Date : 2012
Generisk written by and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2012 with categories.
Generic
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Author : Jeremy A. Greene
language : en
Publisher: Johns Hopkins University Press
Release Date : 2016-09-01
Generic written by Jeremy A. Greene and has been published by Johns Hopkins University Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2016-09-01 with Medical categories.
Greene’s history sheds light on the controversies shadowing the success of generics: problems with the generalizability of medical knowledge, the fragile role of science in public policy, and the increasing role of industry, marketing, and consumer logics in late-twentieth-century and early twenty-first century health care.
Supplement To The Official Journal Of The European Communities
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Author :
language : en
Publisher:
Release Date : 1996
Supplement To The Official Journal Of The European Communities written by and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1996 with Gazettes categories.
The Spectacular Generic
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Author : Cori Hayden
language : en
Publisher: Duke University Press
Release Date : 2022-12-26
The Spectacular Generic written by Cori Hayden and has been published by Duke University Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2022-12-26 with Social Science categories.
In The Spectacular Generic, Cori Hayden examines how generic drugs have transformed public health politics and everyday experiences of pharmaceutical consumption in Latin America. Focusing on the Mexican pharmacy chain Farmacias Similares and its proprietor, Víctor González Torres, Hayden shows how generics have become potent commodities in a postpatent world. In the early 2000s, González Torres, a.k.a. “Dr. Simi,” capitalized on the creation of new markets for generic medicines, selling cheaper copies of leading-brand drugs across Latin America. But Dr. Simi has not simply competed with the transnationals; his enterprise has also come to compete with the Mexican state, reorganizing the provision of medicine and basic health care for millions of people. Hayden juxtaposes this story with Dr. Simi’s less successful efforts in Argentina, where he confronted a radically different configuration of pharmaceutical politics. Building from these diverging trajectories, Hayden illuminates the politics of generic substitution as a question that goes beyond substituting one drug for another. Generic politics can radically reshape the relations among consumers, states, and pharmaceutical markets, even as they have yet to resolve the problems of cost and access.
The Generics Fascination
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Author : Thimo Ludwig Sommerfeld
language : en
Publisher:
Release Date : 2010
The Generics Fascination written by Thimo Ludwig Sommerfeld and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2010 with categories.
Generics And Bioequivalence
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Author : Andre J. Jackson
language : en
Publisher: CRC Press
Release Date : 2019-06-13
Generics And Bioequivalence written by Andre J. Jackson and has been published by CRC Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2019-06-13 with Medical categories.
Published in 1994: This text focuses on the determination of bioequivalence between formulations that are pharmaceutically equivalent and manufactured using acceptable chemistry, manufacturing and controls and in accordance with Good Manufacturing Practices.
Generic Drugs
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Author : Clifford L. Nilsen
language : en
Publisher: iUniverse
Release Date : 2011-01-07
Generic Drugs written by Clifford L. Nilsen and has been published by iUniverse this book supported file pdf, txt, epub, kindle and other format this book has been release on 2011-01-07 with Medical categories.
When you purchase drug products, you dont expect them to be contaminated with antifreeze, industrial chemicals, glass, or dangerous bacteria. But this happens every day when uninformed consumers buy prescription or over-the- counter and behind-the-counter drug products. Armed with the right knowledge, you can avoid the dangers and risks of these drugs and protect yourself and your family. This laypersons guide, written by a drug industry insider, will tell you how the U.S. drug industry works, how drugs are made, where the ingredients come from, and how to identify which drug companies are good and which to avoid. Topics covered include: how generic drugs are approved versus brand name drugs; real stories about how bad drugs have destroyed lives; questionable manufacturing practices; dangers of active ingredients. You dont have to put yourself and your family at risk every time you buy a drug at the store. Make smart buying decisions and take charge of your life with Generic Drugs: A Consumers Self-Defense Guide.
Who Expert Committee On Specifications For Pharmaceutical Preparations
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Author : World Health Organization
language : en
Publisher: World Health Organization
Release Date : 2020-04-21
Who Expert Committee On Specifications For Pharmaceutical Preparations written by World Health Organization and has been published by World Health Organization this book supported file pdf, txt, epub, kindle and other format this book has been release on 2020-04-21 with Medical categories.
Risk Benefit Considerations And Staging Of Differentiated Thyroid Cancer
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Author : Valentina Drozd
language : en
Publisher: Frontiers Media SA
Release Date : 2021-12-20
Risk Benefit Considerations And Staging Of Differentiated Thyroid Cancer written by Valentina Drozd and has been published by Frontiers Media SA this book supported file pdf, txt, epub, kindle and other format this book has been release on 2021-12-20 with Medical categories.
Handbook Of Bioequivalence Testing Second Edition
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Author : Sarfaraz K. Niazi
language : en
Publisher: CRC Press
Release Date : 2014-10-29
Handbook Of Bioequivalence Testing Second Edition written by Sarfaraz K. Niazi and has been published by CRC Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2014-10-29 with Medical categories.
As the generic pharmaceutical industry continues to grow and thrive, so does the need to conduct adequate, efficient bioequivalence studies. In recent years, there have been significant changes to the statistical models for evaluating bioequivalence. In addition, advances in the analytical technology used to detect drug and metabolite levels have made bioequivalence testing more complex. The second edition of Handbook of Bioequivalence Testing has been completely updated to include the most current information available, including new findings in drug delivery and dosage form design and revised worldwide regulatory requirements. New topics include: A historical perspective on generic pharmaceuticals New guidelines governing submissions related to bioequivalency studies, along with therapeutic code classifications Models of noninferiority Biosimilarity of large molecule drugs Bioequivalence of complementary and alternate medicines Bioequivalence of biosimilar therapeutic proteins and monoclonal antibodies New FDA guidelines for bioanalytical method validation Outsourcing and monitoring of bioequivalence studies The cost of generic drugs is rising much faster than in the past, partly because of the increased costs required for approval—including those for bioequivalence testing. There is a dire need to re-examine the science behind this type of testing to reduce the burden of development costs—allowing companies to develop generic drugs faster and at a lower expense. The final chapter explores the future of bioequivalence testing and proposes radical changes in the process of biowaivers. It suggests how the cost of demonstrating bioequivalence can be reduced through intensive analytical investigation and proposes that regulatory agencies reduce the need for bioequivalence studies in humans. Backed by science and updated with the latest research, this book is destined to spark continued debate on the efficacy of the current bioequivalence testing paradigm.