- WHO TRS 1044 Annexure 2…Overview
- This document is a revision of WHO good manufacturing practices for sterile pharmaceutical products, previously published in the WHO Technical Report Series, No. 961, Annex 6, 2011.1 The revision was done in collaboration with the European Union and the Pharmaceutical Inspection Co-operation Scheme (PIC/S). The harmonized text will benefit the national regulatory authorities and manufacturers and save resources, thus improving patients’ access to quality medicines
WHO TRS 1044 ANNEXURE 2- STERILE
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