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
Fermer ce répertoire5. Developing national strategies
Afficher le document5.1 General considerations
Afficher le document5.2 Plan of action
Afficher le document5.3 Monitoring and evaluation
Ouvrir ce répertoire et afficher son contenu6. Specific measures
Ouvrir ce répertoire et afficher son contenu7. Assessment of the problem at the national level
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
 

5.1 General considerations

Counterfeiting of drugs is often undertaken by people and organizations involved in other types of crime, frequently on a large national or even international scale. Measures are needed to prevent the manufacture, supply and distribution of counterfeit drugs. Close cooperation between the various drug control and law enforcement agencies within countries and at the international level is required to ensure that these measures are implemented effectively.

Governments and national DRAs are the organizations with the collective prime responsibility to develop such measures. Legitimate pharmaceutical manufacturers also have a responsibility in the fight against counterfeiting. However, counter-measures are often most effective when they are instituted collaboratively by government and industry.

Experience gained so far has shown that the nature and extent of counterfeiting and the factors facilitating it vary from country to country, and that there is no single or simple way to eliminate the problem. Thus each country has to develop a strategy based on its own situation, taking into account the magnitude of the problem and the available infrastructure, and human and other resources. Even countries with a highly evolved drug regulatory system may not find it easy to design and implement appropriate strategies. Countries with less developed drug regulatory systems and accompanying shortages of trained human resources and funds may have difficulties. It is hoped such countries can be given support and guidance from international organizations, such as WHO, and from selected developed countries with experience in this area.

In the first instance, measures should be directed towards the effective detection of counterfeit drugs in national drug distribution channels, and to preventing them entering these channels. While this may not totally eradicate counterfeit drugs, it should substantially reduce the exposure of the population to the risks associated with these products. Although counterfeit drugs are known to exist in the national drug distribution channels of many countries, their extent and nature are not fully known. An assessment of the current situation is therefore the first step, ensuring that a clear distinction is made between substandard and counterfeit products. Measures should also include procedures to improve drug control systems and cooperation in enforcing existing legislation.

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Dernière mise à jour: le 24 avril 2012