The Qualified Person for Pharmacovigilance for Europe

Abstract A decade after the legal requirement for a qualified person (QP) for pharmacovigilance for Europe for each pharmaceutical company was promulgated, the exact obligations of the QP remain contentious. This paper reviews the responsibilities of the QP, as set out in legislation and guidelines,...
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Author:

Brown, Elliot G. [VerfasserIn]

Format:

Electronic Article

Language:

English

Published:

2005

Subjects:

European Union

Competent Authority

Marketing Authorisation

Qualified Person

Adverse Event Report

Containing Work:

Enthalten in: Pharmaceutical medicine - Auckland : Wolters Kluwer Health Adis, 2008, 19(2005), 1 vom: Feb., Seite 7-14

Containing Work:

volume:19 ; year:2005 ; number:1 ; month:02 ; pages:7-14

Links:

Volltext [lizenzpflichtig]

DOI / URN:

10.2165/00124363-200519010-00003

Catalog id:

SPR035360291

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