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Law, medicine, and medical technology : cases and materials / Lars Noah, Professor of Law, University of Florida.

Por: Series University casebook seriesEditor: St. Paul, MN : Foundation Press, 2017Edición: Fouth editionDescripción: xli, 1343 pages ; 26 cmTipo de contenido:
  • text
Tipo de medio:
  • unmediated
Tipo de soporte:
  • volume
ISBN:
  • 9781634599405
  • 1634599403
Tema(s): Clasificación LoC:
  • KF 3821 .A7 .N63 2017
Contenidos:
Part I. Government regulation -- FDA control : preliminaries -- Development and testing of experimental therapies -- Premarket approval and postmarket surveillance -- Dissemination of product information -- Part II. Tort liability -- Products liability : preliminaries -- Production failures -- Informational defects -- Utilization errors and medical malpractice -- Part III. Economics and innovation -- Pricing and payment systems -- Managing incentives for innovation -- Evolving medical technologies.
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Imagen de cubierta Tipo de ítem Biblioteca actual Biblioteca de origen Colección Ubicación en estantería Signatura topográfica Materiales especificados Info Vol URL Copia número Estado Notas Fecha de vencimiento Código de barras Reserva de ítems Prioridad de la cola de reserva de ejemplar Reservas para cursos
Libro Biblioteca de Derecho Mons. Fremiot Torres Oliver Colección General biblioteca derecho KF 3821 .A7 N63 2017 (Navegar estantería(Abre debajo)) Disponible 70000000904790
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Descripciones mejoradas de Syndetics:

Five years after publication of the third edition, and reflecting the dynamic nature of the pharmaceutical and medical device industries (as well as the many different areas of law that pertain to the management of these medical technologies), the Fourth Edition incorporates the latest legislative, regulatory, and judicial developments, describes recent scientific advances, and excerpts or references new scholarly contributions to this broad field (the wealth of citations should facilitate use in a seminar setting). Measured by volume, more than 20% of the previous edition has been replaced with new material. The latest edition retains the same basic thematic approach and modular structure of the original, which allows instructors to pick and choose the materials to cover based on their own tastes and areas of expertise.

Includes bibliographical references (pages ix-xi) and index.

Part I. Government regulation -- FDA control : preliminaries -- Development and testing of experimental therapies -- Premarket approval and postmarket surveillance -- Dissemination of product information -- Part II. Tort liability -- Products liability : preliminaries -- Production failures -- Informational defects -- Utilization errors and medical malpractice -- Part III. Economics and innovation -- Pricing and payment systems -- Managing incentives for innovation -- Evolving medical technologies.

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