Directive 2001/20/EC on Good Clinical Practice in Clinical Trials: Overview with Reference to Pharmacovigilance

Author: Joy I. Chukwujindu1

Source: International Journal of Pharmaceutical Medicine, Volume 18, Number 1, 2004 , pp. 9-12(4)

Publisher: Adis International

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Keywords: Pharmaceutical industry; Regulatory process

Document Type: Commentary

Affiliations: 1: Pharmacovigilance Department, Akos Clinical Development Limited, Harpenden, UK

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