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EMEA: Questions/answers on Quality of IMPs - Inspections/QWP

16.02.2009
EMEA:
Questions/answers on Quality of IMPs - Inspections/QWP.
Reference to relevant paragraphs of the Guideline on the Requirements to the Chemical and Pharmaceutical Quality Documentation Concerning Investigational Medicinal Products in Clinical Trials (CHMP/QWP/185401/2004)) final is given for each question