Counterfeit Drugs
(1999; 61 pages) [French] [Spanish] Voir le document au format PDF
Table des matières
Afficher le documentExecutive Summary
Ouvrir ce répertoire et afficher son contenu1. Introduction
Afficher le document2. Overview of the problem
Afficher le document3. Impact on public health
Afficher le document4. Factors facilitating counterfeiting
Ouvrir ce répertoire et afficher son contenu5. Developing national strategies
Ouvrir ce répertoire et afficher son contenu6. Specific measures
Fermer ce répertoire7. Assessment of the problem at the national level
Afficher le document7.1 Approaches
Afficher le document7.2 Sampling procedures
Afficher le document7.3 Limitations
Ouvrir ce répertoire et afficher son contenu8. Inspection when pharmaceutical products are suspected to be counterfeit, spurious or substandard
Ouvrir ce répertoire et afficher son contenu9. Test methods
Ouvrir ce répertoire et afficher son contenu10. Developing training programmes: inspection and examination of counterfeit pharmaceuticals
Afficher le document11. Conclusion
Afficher le documentReferences
Afficher le documentSelected further reading
Afficher le documentAcknowledgements
Afficher le documentGlossary
 

7. Assessment of the problem at the national level

As indicated in section 5, it is important to know the magnitude and nature of drug counterfeiting in a country when designing strategies to combat the problem and determining priorities for implementation. The numerous studies conducted in many countries on the quality of available pharmaceutical products were not specifically designed to gather information on counterfeit drugs, and have therefore provided few accurate data in this area. Further information on the risks of exposure to treatments with poor quality drug products and, more specifically, with counterfeit products is also required.

Before embarking on a national study to assess drug counterfeiting, countries should consider appropriate methods and procedures, prepare a practical guide(s) for the collection of samples and decide how the results will be issued. The results of such studies performed in other countries may be useful in designing protocols. If external experts are performing the study, they should discuss all these aspects with the appropriate national authorities prior to implementation.

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Dernière mise à jour: le 24 avril 2012