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Home » EMEA Amends Quality Review of Documents Templates
EMEA Amends Quality Review of Documents Templates
October 16, 2009
Drugmakers using the European Medicines Agency’s (EMEA) centralized procedure to submit new applications for marketing authorizations should comply with a revision of the Quality Review of Documents (QRD) template as soon as possible, the agency says. Includes the full text of EC Guideline on Summary of Product Characteristics.
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