Therapeutic Goods Regulations 1990 PDF Download

Author: Australia. Attorney-General's Department. Office of Legislative Drafting and Publishing
Publisher:
ISBN:
Category : Drugs
Languages : en
Pages : 266

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Author: Australia
Publisher:
ISBN: 9780642419439
Category : Drugs
Languages : en
Pages : 202

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Author: Australia
Publisher:
ISBN:
Category : Drugs
Languages : en
Pages : 13

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Author: John McEwan
Publisher:
ISBN: 9780980422900
Category : Drugs
Languages : en
Pages : 170

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Author: Australia
Publisher:
ISBN:
Category : Drugs
Languages : en
Pages : 44

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Author: World Health Organization
Publisher:
ISBN:
Category : Business & Economics
Languages : en
Pages : 32

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"Resolution WHA41.17 adopted by the Forty-first World Health Assembly, 13 May 1988" -- p.1.

Author: National Academies of Sciences, Engineering, and Medicine
Publisher: National Academies Press
ISBN: 0309498635
Category : Medical
Languages : en
Pages : 169

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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.

Author: Graeme A. Hodge
Publisher: Edward Elgar Publishing
ISBN: 184720872X
Category : Technology & Engineering
Languages : en
Pages : 445

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This is an insightful collection by leading thinkers in both regulation and nanotechnology. It confronts new technological challenges with fresh regulatory insight. John Braithwaite, Australian National University Our growing ability to manufacture materials at the atomic scale will change our lives for the better, and tomorrow s nano-economy will outperform today s information age. Or so its proponents claim. Others maintain that a future dominated by commercial incentives risks a toxicological nightmare to rival the sorry global story of asbestos. This important volume is a timely contribution to increasing international calls to regulate nanotechnologies. By investigating the ways in which we could regulate these advances, and what we are learning from regulating existing technologies, such as biotechnologies and information technologies, the book debates the roles of government, business actors and the professions in protecting and enhancing the lives of citizens. In placing particular emphasis on the lessons of earlier technology advances, this book is unique in its broad consideration of the ethical, legal and social issues entwined within the development of the nanotechnology family. The multi-jurisdictional and interdisciplinary nature of the book will appeal to governments, academics, and civil societies across many parts of the world, while also remaining accessible to informed readers with an interest in nanotechnology and the policy and governance issues associated with technology development and regulation.

Author: National Health and Medical Research Council (Australia)
Publisher:
ISBN: 9780648464426
Category : Human rights
Languages : en
Pages : 0

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"The purpose of the National Statement is to promote ethically good human research. Fulfilment of this purpose requires that participants be accorded the respect and protection that is due to them. It also involves the fostering of research that is of benefit to the community. The National Statement is therefore designed to clarify the responsibilities of: institutions and researchers for the ethical design, conduct and dissemination of results of human research ; and review bodies in the ethics review of research. The National Statement will help them to meet their responsibilities: to identify issues of ethics that arise in the design, review and conduct of human research, to deliberate about those ethical issues, and to justify decisions about them"--Page 6.

Author: United States. Federal Trade Commission. Bureau of Consumer Protection
Publisher:
ISBN:
Category : Advertising
Languages : en
Pages : 32

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