The following guideline can be ordered through the address listed in the "Source/Publisher"-category. In cases in which you can order through the Internet we have established a hyperlink.

Eudralex Volume 3 Requirements to the Chemical and Pharmaceutical Quality Documentation Concerning Investigational Medicinal Products in Clinical Trials (CHMP/QWP/185401/2004)

Origin/Publisher:

EMEA 7 Westferry Circus, Canary Wharf, London, E14 4HB, UK Tel (44-20-7) 418 8400, Fay (44-20-7) 418 85 95 info@ema.europa.eu; http://www.emaea.europa.eu

Document Type:
Guideline
Content:
Requirements on the documentation of investigational medicinical products with has to be submitted to the authorities prior to the beginning of the clinical trials.

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