European regulation of medical devices and pharmaceuticals : regulatee expectations of legal certainty
European regulation of medical devices and pharmaceuticals : regulatee expectations of legal certainty
Law of Europe > Regional organization and integration (Europe) > The European Communities. Community law > Medical legislation > Special topics, A-Z > Medical instruments and apparatus. Medical devices > Periodicals > KJE6229
Edition Details
- Creator or Attribution (Responsibility): Nupur Chowdhury
- Language: English
- Jurisdiction(s): Switzerland
- Publication Information: Cham : Springer, 2014
- Publication Type (Medium): Electronic books
- Material: Document, Internet resource
- Type: Internet Resource, Computer File
- Permalink: http://books.lawlegal.eu/european-regulation-of-medical-devices-and-pharmaceuticals-regulatee-expectations-of-legal-certainty/ (Stable identifier)
Additional Format
Print version:
Short Description
1 online resource (XIII, 185 pages) : ILlustrations
Purpose and Intended Audience
Useful for students learning an area of law, European regulation of medical devices and pharmaceuticals : regulatee expectations of legal certainty is also useful for lawyers seeking to apply the law to issues arising in practice.
Research References
- Providing references to further research sources: Search
More Options
- Find it at other libraries via WorldCat/OCLC
- Find European regulation of medical devices and pharmaceuticals : regulatee expectations of legal certainty in Google Books
- Find European regulation of medical devices and pharmaceuticals : regulatee expectations of legal certainty in Open Library
Bibliographic information
- Publisher: Springer
- Responsable Person: Nupur Chowdhury.
- Publication Date: 2014
- Country/State: Switzerland
- Number of Editions: 9 editions
- First edition Date: 2014
- Last edition Date: 2014
- Languages: English, German
- Library of Congress Code: KJE6229
- Dewey Code: 344.4042
- ISBN: 9783319045948 3319045946 3319045938 9783319045931
- OCLC: 879374253
Main Contents
1. Introduction
2. Conceptualizing Multilevel Regulation
3. Reconceptualizing Legal Certainty: From a Principle of Positive Law to Regulatee Expectations
4. Explanation of Methodological Choices
5. Pilot Study of Regulatory Uncertainty in Marketing Authorization of Medical Products in Europe
6. Case Study on Medical Devices Regulation in Europe
7. Case Study on Pharmaceutical Regulation in Europe
8. Case Study on Borderline Medical Products in Europe
9. Conclusion.
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