TRS 1052 - Annex 4: WHO good practices for pharmaceutical quality control laboratories
26 April 2024
| Technical document
Overview
This guideline is consistent with the requirements of the WHO good manufacturing practices for pharmaceutical products (1) and international standard ISO/IEC 17025:2017 (2), providing detailed guidance for laboratories performing quality control testing of medicines.WHO Team
Access to Medicines and Health Products (MHP),
Health Product Policy and Standards (HPS),
Norms and Standards for Pharmaceuticals (NSP),
Technical Standards and Specifications (TSS)
Number of pages
88