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
Key:
- Free Content
- New Content
- Subscribed Content
- Free Trial Content
Keywords: Pharmaceutical industry; Regulatory process
Document Type: Commentary
Affiliations: 1: Pharmacovigilance Department, Akos Clinical Development Limited, Harpenden, UK
Key:
- Free Content
- New Content
- Subscribed Content
- Free Trial Content

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