European regulation of consumer product safety
著者
書誌事項
European regulation of consumer product safety
Oxford University Press, 2005
大学図書館所蔵 全17件
  青森
  岩手
  宮城
  秋田
  山形
  福島
  茨城
  栃木
  群馬
  埼玉
  千葉
  東京
  神奈川
  新潟
  富山
  石川
  福井
  山梨
  長野
  岐阜
  静岡
  愛知
  三重
  滋賀
  京都
  大阪
  兵庫
  奈良
  和歌山
  鳥取
  島根
  岡山
  広島
  山口
  徳島
  香川
  愛媛
  高知
  福岡
  佐賀
  長崎
  熊本
  大分
  宮崎
  鹿児島
  沖縄
  韓国
  中国
  タイ
  イギリス
  ドイツ
  スイス
  フランス
  ベルギー
  オランダ
  スウェーデン
  ノルウェー
  アメリカ
注記
Includes bibliographical references (p. [297]-308) and index
内容説明・目次
内容説明
This book examines the European Community legislation that regulates the safety of consumer products. Hodges surveys the extent to which this legislation aims to and succeeds in achieving safety for a wide range of products. There are different legal requirements for medicines, machines, electronics, toys and so on, which employ different regulatory mechanisms, including pre-marketing assessment, provision of information, control of the manufacturing environment,
post-marketing obligations on producers and authorities, and obligations on distributors and users. Hodges compares the various mechanisms relating to medicinal products, products covered by 'New Approach' Directives, cosmetics, biocides, tobacco products, and consumer products covered by the General
Product Safety Directive, and asks why particular mechanisms are used, or not used for different products.
The book then moves on to consider what is meant by product 'safety', demonstrating the relativity of this concept. Hodges highlights an important problem: that consumers, the media, and experts can all have differing ideas on the level of safety that is relevant and acceptable. Hodges contends that the systems are in need of review, to ensure they work effectively and give value for money. In some cases, there is an need for more or less control. He argues for more systematic collection of
safety data, and for consistecy in surveillance and enforcement mechanisms across Europe, pointing towards the need for a European Product Safety Agency.
目次
- Table of Legislation
- Table of Cases
- List of Figures
- List of Tables
- List of Abbreviations
- Introduction
- 1. Theoretical aspects of regulation
- PART ONE: DESCRIPTION OF THE MAIN REGULATORY SYSTEMS AT COMMUNITY LEVEL
- 2. Introduction
- 3. The limits on the Community's jurisdictional competence in product safety legislation
- 4. Medicinal products
- 5. New Approach products
- 6. Biocides, cosmetics, tobacco, and general consumer products
- PART TWO: PROCEDURAL MECHANISMS FOR SAFETY
- 7. Introduction
- 8. Pre-market assessment: authorization to market
- 9. Control of the manufacturing environment and process
- 10. Providing information
- 11. Producers' Post-marketing obligations
- 12. The role of the authorities in post-marketing safety
- 13. Control of distribution
- 14. Obligations on users
- 15. Conclusions on safety mechanisms
- PART THREE: THEORETICAL ISSUES AND CONCLUSIONS
- 16. Introduction
- 17. The Community institutions involved and their mechanisms of governance
- 18. Safety and risk
- 19. Conclusions
- APPENDICES
- Appendix 1 The Pharmacovigilance System
- Appendix 2 Statistics on the safety of general consumer products
- Appendix 3 Statistics on the safety of medicinal products
- Appendix 4 Statistics on the safety of electrical products
- Appendix 5 Modules for conformity assessment procedures under the New Approach
- BIBLIOGRAPHY
- INDEX
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