TRS 1025 - Annex 2: IAEA - WHO good manufacturing practices for radiopharmaceutical products
Annex 2, WHO Technical Report Series 1025, 2020
30 September 2020
| Technical document
Overview
This guideline provides a general overview of the minimum good manufacturing practices (GMP) requirements for radiopharmaceutical products. The main principles of GMP are described in detail in the WHO guidelines related to pharmaceutical products (1, 2), as well as in those for sterile pharmaceutical products (3).
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
16