WHO Good Manufacturing Practices for Sterile Pharmaceutical Products. WHO Technical Report Series, No. 961, 2011, Annex 6
(2011; 24 pages)

Resumen

Following implementation of these WHO good manufacturing practices (GMP) guidelines within the context of the WHO Prequalification of Medicines Programme, clarifying, editorial modifications have been proposed. These changes were adopted for maintenance purposes. In order to ease reading the full guideline has been reproduced again as an Annex to the current report of the WHO Expert Committee on Specifications for Pharmaceutical Preparations.

 
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