A History Of Therapeutic Goods Regulation In Australia
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A History Of Therapeutic Goods Regulation In Australia
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Author : John McEwan
language : en
Publisher:
Release Date : 2007
A History Of Therapeutic Goods Regulation In Australia written by John McEwan and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2007 with Drugs categories.
Review Of Business Regulations
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Author :
language : en
Publisher:
Release Date : 1989
Review Of Business Regulations written by and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1989 with Pharmaceutical industry categories.
Therapeutic Goods Act 1966
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Author : Australia
language : en
Publisher:
Release Date : 1990-01-01
Therapeutic Goods Act 1966 written by Australia and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1990-01-01 with Capsules (Pharmacy) categories.
Therapeutic Goods Act 1989
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Author :
language : en
Publisher:
Release Date : 1992
Therapeutic Goods Act 1989 written by and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1992 with Drugs categories.
Australian Medical Device Requirements
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Author : Therapeutic Goods Administration (Australia)
language : en
Publisher:
Release Date : 1998
Australian Medical Device Requirements written by Therapeutic Goods Administration (Australia) and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1998 with Medical instruments and apparatus categories.
Therapeutic Goods Administration Tga
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Author :
language : en
Publisher:
Release Date : 1999
Therapeutic Goods Administration Tga written by and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1999 with Medical instruments and apparatus categories.
The Therapeutic Goods Administration (TGA) is a Division of the Department of Health and Ageing, Australia and is responsible for administering the provisions of the Therapeutic Goods Act. This site provides information about the regulations and control of prescription drugs, over the counter medications and medical devices within Australia. Also included are links to information on issues associated with [agricultural and environmental] chemicals, complementary medicines and gene technology.
Requirements For The Supply Of Therapeutic Devices Under The Therapeutic Goods Act 1989
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Author :
language : en
Publisher:
Release Date : 1993
Requirements For The Supply Of Therapeutic Devices Under The Therapeutic Goods Act 1989 written by and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1993 with Australia categories.
Regulating Medicines In A Globalized World
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Author : National Academies of Sciences, Engineering, and Medicine
language : en
Publisher: National Academies Press
Release Date : 2020-04-25
Regulating Medicines In A Globalized World written by National Academies of Sciences, Engineering, and Medicine and has been published by National Academies Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2020-04-25 with Medical categories.
Globalization is rapidly changing lives and industries around the world. Drug development, authorization, and regulatory supervision have become international endeavors, with most medicines becoming global commodities. Drug companies utilize global supply chains that often include facilities in countries with inconsistent regulations from those of the United States, perform pivotal trials in multiple countries to support registration submissions in various jurisdictions, and subsequently market their medicines throughout most of the world. These companies operate across borders and require individual national regulators to ensure that drugs authorized for use in their countries are safe and effective, and appropriate for their health care system and their population. This process involves significant resources and often duplicative work. It is important to consider how this process can be improved in order to better allocate resources, time, and efforts to improve public health. Regulating Medicines in a Globalized World: The Need for Increased Reliance Among Regulators considers the role of mutual recognition and other reliance activities among regulators in contributing to enhancing public health. This report identifies opportunities for leveraging reliance activities more broadly in order to potentially impact public health globally. Key topics in this report include the job of medicines regulators in today's world, what policy makers need to know about today's regulatory environment, stakeholder views of recognition and reliance, as well as removing impediments and facilitating action for greater recognition and reliance among regulatory authorities.
Medical Device Regulations
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Author : Michael Cheng
language : en
Publisher: World Health Organization
Release Date : 2003-09-16
Medical Device Regulations written by Michael Cheng 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 2003-09-16 with Medical categories.
The term 'medical devices' covers a wide range of equipment essential for patient care at every level of the health service, whether at the bedside, at a health clinic or in a large specialised hospital. Yet many countries lack access to high-quality devices, particularly in developing countries where health technology assessments are rare and there is a lack of regulatory controls to prevent the use of substandard devices. This publication provides a guidance framework for countries wishing to create or modify their own regulatory systems for medical devices, based on best practice experience in other countries. Issues highlighted include: the need for harmonised regulations; and the adoption, where appropriate, of device approvals of advanced regulatory systems to avoid an unnecessary drain on scarce resources. These approaches allow emphasis to be placed on locally-assessed needs, including vendor and device registration, training and surveillance and information exchange systems.
Tgs Information Kit An Introductory Guide To The Regulatory Processes For Registering And Listing Medicines In Australia
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Author :
language : en
Publisher:
Release Date : 1999
Tgs Information Kit An Introductory Guide To The Regulatory Processes For Registering And Listing Medicines In Australia written by and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1999 with categories.