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Eudralex Volume 3 Requirements to the Chemical and Pharmaceutical Quality Documentation Concerning Investigational Medicinal Products in Clinical Trials
Short Title:
EMA/CHMP/QWP/545525/2017
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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