Quality Assurance of Pharmaceuticals - A Compendium of Guidelines and Related Materials - Volume 1
(1997; 248 pages) [French] Voir le document au format PDF
Table des matières
Ouvrir ce répertoire et afficher son contenuIntroduction
Ouvrir ce répertoire et afficher son contenu1. National drug regulation
Ouvrir ce répertoire et afficher son contenu2. Product assessment and registration
Ouvrir ce répertoire et afficher son contenu3. Distribution
Ouvrir ce répertoire et afficher son contenu4. The international pharmacopoeia and related activities
Ouvrir ce répertoire et afficher son contenu5. Basic tests
Ouvrir ce répertoire et afficher son contenu6. Laboratory services
Fermer ce répertoire7. International trade in pharmaceuticals
Ouvrir ce répertoire et afficher son contenuGuidelines for implementation of the WHO Certification Scheme on the Quality of Pharmaceutical Products Moving in International Commerce1
Afficher le documentWorld Health Assembly resolution WHA50.3: Guidelines on the WHO Certification Scheme on the Quality of Pharmaceutical Products Moving in International Commerce
Afficher le documentGuidelines on import procedures for pharmaceutical products1
Ouvrir ce répertoire et afficher son contenu8. Counterfeit products
Ouvrir ce répertoire et afficher son contenu9. Training
Afficher le documentSelected WHO publications of related interest
Afficher le documentBack cover
 

World Health Assembly resolution WHA50.3: Guidelines on the WHO Certification Scheme on the Quality of Pharmaceutical Products Moving in International Commerce

The Fiftieth World Health Assembly,

Taking note of previous resolutions on WHO’s Certification Scheme on the Quality of Pharmaceutical Products Moving in International Commerce, and particularly resolutions WHA45.29 and WHA49.14;

Having reviewed the revised guidelines on implementation of the Certification Scheme which are the result of field trials in a number of WHO Member States and discussions during the sixth and seventh biennial International Conferences of Drug Regulatory Authorities;1

1 WHO Technical Report Series, No. 863, 1996, Annex 10.

Believing that the adoption of the revised guidelines will provide an important instrument in support of drug registration in the importing country by ensuring access to transparent information on the regulatory status of the pharmaceutical product in the exporting country and the true origin of products to be imported,

1. ENDORSES the guidelines for implementation of the WHO Certification Scheme on the Quality of Pharmaceutical Products Moving in International Commerce and model certification forms annexed to the guidelines;

2. URGES Member States:

(1) to implement these guidelines, to request WHO-type certificates in the form contained in the guidelines and to issue the certificates in the form proposed, as from 1 January 1998;

(2) to inform the Director-General of their intent to apply the Scheme and of any significant reservations they intend to express relating to their participation as provided for in article 2.1 of the guidelines.

vers la section précédente vers la section suivante
 

Dernière mise à jour: le 3 mai 2013