top of page

WHO

Guidelines on pre-market approvals requirements-

WHO 4-annex-2-gmp-for-sterile-pharmaceutical-products

WHO annex1-goodpractices-Pharmaceuticalqualitycontrol-laboratories

WHO annex2-main principle

WHO annex2-points-to-consider-when-incl-hbels-in-cleaning-validation

WHO annex3-gmp-water-for-pharmaceuticals-use

WHO annex3-good-manufacturing-practices-for-radiopharmaceutical-products-(1)

WHO annex4-guideline-on-data-integrity

WHO annex4-technology-transfer-in-pharmaceutical-manufacturing

WHO annex5-good-manufacturing-practices-for-medicinal-gases

WHO annex6-good-practices-for-research-and-dev-facilities-of-pharmaceutical-products

WHO annex7-good-manufacturing-practices-for-investigational-products

WHO GMP ANNEX2_27.01.23

WHO_annex3_who-gmp-for-pharmaceutical-products-containing-hazardous-substances

WHO_gmp-for active ingredients

WHO-annex1-herbal processing practices for herbal medicines

WHO-annex2-guideline on good manufacturing practices

WHO-annex2-quality-risk-management

WHO-annex2-who-gmp-manufacture-herbal-medicines

WHO-annex03-gmp-for-biological-products

WHO-annex3-gmp-guidelines on validation

WHO-annex3-Production of WFI by means other than Distillation

WHO-annex4-General guidance on hold-time studies

WHO-annex4-gmp- for blood establishments (jointly with the Expert Committee on Biological Standardization)

WHO-annex5--gmp-for-the-manufacture-of-pharmaceutical-excipients

WHO-annex6-environmental aspects of manufacturing for the prevention of antimicrobial resistance

WHO-annex7-guidelines for preparation of a contract research organization master file

WHO-annex8-who-gmp-Guidelines on heating, ventilation and air-conditioning systems for non-sterile pharmaceutical products

WHO-annex9-packaging for pharmaceutical products

WHO-good-manufacturing-practices-for-HVAC-systems-for-non-sterile-pharmaceutical-products-(part-2)-interpretation-of-guidelines

bottom of page