1. Introduction
2. General policy
3. Quality control
specifications and tests
4. Quality control
international reference materials
5. Quality control
national laboratories
6. Quality assurance
good manufacturing practices (GMP)
7. Quality assurance
inspection
8. Quality assurance
distribution and trade-related
9. Quality assurance
risk analysis
10. Quality assurance
drug supply
11. Quality assurance
storage
12. International Nonproprietary Names (INNs) Programme
13. Miscellaneous
Annex 1. Recommendations on risk of transmitting animal spongiform encephalopathy agents via medicinal products
Annex 2. The International Pharmacopoeia: revised concepts and future perspectives
Annex 3. Guidelines on good manufacturing practices for radiopharmaceutical products
Annex 4. Good manufacturing practices for pharmaceutial products: main prinicples
Annex 5. Model certificate of good manufacturing practices
Annex 6. Guidance on good manufacturing practices (GMP): inspection report
Annex 7. Application of hazard analysis and critical control point (HACCP) method to pharmaceuticals
Annex 8. Procedure for assessing the acceptability, in principle, of pharmaceutical products for purchase by United Nations agencies
Annex 9. Guide to good storage practices for pharmaceuticals.