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Informed Consent in Europe

Legal, Ethical and Clinical Perspectives

C.H.BECK

ISBN 978-3-406-64857-1

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ca. 120,00 €

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Bibliografische Daten

Handbuch

Buch. Hardcover (Leinen)

2024

In englischer Sprache

(In Gemeinschaft mit Hart Publishing, Oxford und Nomos Verlagsgesellschaft, Baden-Baden)

Umfang: Rund 300 S.

Format (B x L): 16,0 x 24,0 cm

Verlag: C.H.BECK

ISBN: 978-3-406-64857-1

Weiterführende bibliografische Daten

Das Werk ist Teil der Reihe: Kooperationswerke Beck - Hart - Nomos

Produktbeschreibung

Zum Werk
Informed consent is intrinsically connected to a person's autonomy. Consent is a process to allow the patient (or data subject) to express his wishes and choices in an informed and autonomous way.
In order to fulfil its role as a mechanism to protect the patient, it is thus of crucial importance that the informed consent procedure is as concise, precise, clear and personalised as possible.
European regulatory documents obliging to obtain in-formed consent seem to connect the same ethical and legal idea to very different legal requirements. The different legal concepts might boost the tendency that consent is not so much seen as a means to protect the patient's autonomy but more as a cumbersome procedure needed to shrink liabilities and protect the physician.
This book - based on research undertaken in an FP-7 project - gives an overview on the concept of informed consent as well as current and upcoming issues of getting, giving and managing informed consent.

Vorteile auf einen Blick

Zielgruppe
Medizinrechtler; Verbände; Rechtsanwälte.

Autorinnen und Autoren

Kundeninformationen

Bereits angekündigt u.d.T. "Law and Ethics of Informed Consent"

Informed consent is intrinsically connected to a person’s autonomy. Consent is a process to allow the patient (or data subject) to express his wishes and choices in an informed and autonomous way.


In order to fulfil its role as a mechanism to protect the patient, it is thus of crucial importance that the informed consent procedure is as concise, precise, clear and personalised as possible.


European regulatory documents obliging to obtain informed consent seem to connect the same ethical and legal idea to very different legal requirements. The different legal concepts might boost the tendency that consent is not so much seen as a means to protect the patient’s autonomy but more as a cumbersome procedure needed to shrink liabilities and protect the physician.


This book — based on research undertaken in an European project — gives an overview on the concept of informed consent as well as current and upcoming issues of getting, giving and managing informed consent.

Produktsicherheit

Hersteller

Verlag C.H.Beck GmbH & Co. KG

Wilhelmstraße 9
80801 München, Deutschland

produktsicherheit@beck.de

www.beck.de

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