Informed Consent in Europe
Legal, Ethical and Clinical Perspectives
C.H.BECK
ISBN 978-3-406-64857-1
Standardpreis
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
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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