European regulation of medical devices and pharmaceuticals : regulatee expectations of legal certainty

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

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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.

Structured Subjects (Headings):

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