WHO Good Manufacturing Practices For Sterile Pharmaceutical Products, WHO TRS 961, 2011 Annex 6
Introduction:
Following implementation of these WHO good manufacturing practices (GMP) guidelines (1) 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.
Click on the any titles below for complete guidelines
TABLE OF CONTENTS
4. Manufacture of sterile preparations
7. Aseptic processing and sterilization by filtration
13. Finishing of sterile products
WHO GMP For Sterile Pharmaceutical Products | Annex 6
