Regulation of Medical Products - Dope, Drugs and Devices

This book develops a theoretical framework for examining and assessing the regulatory arrangements for medical products.

List of contents

1. Introduction 2. The Foundations of the Regulation of Medical Products 3. A Constant Dialogic Approach to Political Legitimacy 4. Voices of Change: Regulatory Reform of Medicinal Cannabis in Australia 5. A Normative Void: The Regulation of Medical Abortion in Australia 6. Shouting to Be Heard: The Regulation of Urogynaecological Mesh Devices in Australia 7. Regulatory Challenges, Courage and Evolution 8. Conclusion

About the author

Penny Gleeson is Lecturer at Deakin Law School, Melbourne, Australia.

Summary

This book develops a theoretical framework for examining and assessing the regulatory arrangements for medical products.

Product details

• Authors: Penny Gleeson, Penny (Deakin University Gleeson
• Publisher: Taylor & Francis Ltd.
• Languages: English
• Product format: Hardback
• Released: 31.12.2024
• EAN: 9781032277127
• ISBN: 978-1-0-3227712-7
• No. of pages: 276
• Series: Law, Science and Society
• Subjects: Humanities, art, music > Education > Social education, social work; Social sciences, law, business > Media, communication > Communication science; Sociology, Science: general issues, SOCIAL SCIENCE / Sociology / General, MEDICAL / Public Health, SOCIAL SCIENCE / Disease & Health Issues, LAW / Medical Law & Legislation, POLITICAL SCIENCE / Public Affairs & Administration, SCIENCE / Research & Methodology, Personal & public health, Illness & addiction: social aspects, Systems of law, Public Administration, Medical & healthcare law, Medical Sociology, Health, illness and addiction: social aspects, Personal and public health / health education, Medicolegal issues, Medical and healthcare law, Scientific research, Science Funding & Policy, Science funding and policy, Research methods: general, Health, illness or addiction: social aspects