£48.55

Springer Das europäische Arzneimittelrecht: Zentrale Rechtsfragen des Arzneimittelzulassungsverfahrens

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Description

Im Fokus des Buches von Regina Kröll steht die Analyse des gesamten Zulassungsverfahrens, vom Anwendungsbereich über die Besonderheiten des Zulassungsantrages und den Verfahrensablauf bis zur Phase nach Erteilung der Zulassung. Beleuchtet werden außerdem die Entwicklung des europäischen Arzneimittelrechts, die Übertragung von Befugnissen an nachgeordnete Unionseinrichtungen sowie Rechtsgrundlagen, Aufbau und Arbeitsweise der Europäischen Arzneimittelagentur, wobei auch der Problemkreis der Legitimität, Unabhängigkeit und Transparenz thematisiert wird. Den Abschluss bilden Erwägungen zum Rechtsschutz. From the Back Cover Im Fokus des Buches von Regina Kröll steht die Analyse des gesamten Zulassungsverfahrens, vom Anwendungsbereich über die Besonderheiten des Zulassungsantrages und den Verfahrensablauf bis zur Phase nach Erteilung der Zulassung. Beleuchtet werden außerdem die Entwicklung des europäischen Arzneimittelrechts, die Übertragung von Befugnissen an nachgeordnete Unionseinrichtungen sowie Rechtsgrundlagen, Aufbau und Arbeitsweise der Europäischen Arzneimittelagentur, wobei auch der Problemkreis der Legitimität, Unabhängigkeit und Transparenz thematisiert wird. Den Abschluss bilden Erwägungen zum Rechtsschutz. Der Inhalt Die Entwicklung des Europäischen Arzneimittelrechts Der Arzneimittelbegriff Die Europäische Arzneimittelagentur Das Zulassungsverfahren  Rechtsschutz  Die Zielgruppen Dozierende und Studierende der Rechtswissenschaften Rechtsanwälte und Führungskräfte aus der Pharmaindustrie Die Autorin Dr. Regina Kröll ist Rechtsanwaltsanwärterin und in den Bereichen öffentliches Wirtschaftsrecht und Europarecht tätig. About the Author Dr. Regina Kröll ist Rechtsanwaltsanwärterin und in den Bereichen öffentliches Wirtschaftsrecht und Europarecht tätig.

Product Specifications

Format
paperback
Domain
Amazon UK
Release Date
10 February 2017
Listed Since
06 February 2017

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