Annex 1
Guidelines and guidance texts adopted by the Expert Committee on Specifications for Pharmaceutical Preparations
Annex 2
WHO good manufacturing practices for excipients used in pharmaceutical products
Annex 3
IAEA/WHO good manufacturing practices for in house cold kits for radiopharmaceutical preparations
Annex 4
WHO good practices for pharmaceutical quality control laboratories
Annex 5
WHO/UNFPA female condom generic specification
Annex 6
WHO Biowaiver List: proposal to waive in vivo bioequivalence requirements for WHO Model List of Essential Medicines immediate-release, solid oral dosage forms
Annex 7
WHO guideline on Biopharmaceutics Classification System-based biowaivers
Annex 8
Multisource (generic) pharmaceutical products: guidelines on registration requirements to establish interchangeability