Proceedings of the Ninth International Conference of Drug Regulatory Authorities (ICDRA) - Berlin, Germany 25-29 April 1999
(1999; 102 pages) Voir le document au format PDF
Table des matières
Ouvrir ce répertoire et afficher son contenuOpening Ceremony
Ouvrir ce répertoire et afficher son contenuGood regulatory practice
Ouvrir ce répertoire et afficher son contenuGood certification practice
Fermer ce répertoireCounterfeit drugs: challenges and solutions
Afficher le documentIllicit pharmaceutical markets
Afficher le documentThe situation of counterfeit drugs
Afficher le documentRecommendations
Ouvrir ce répertoire et afficher son contenuCurrent issues in regulation and quality
Ouvrir ce répertoire et afficher son contenuInternational Conference on Harmonization: implementation and implications
Ouvrir ce répertoire et afficher son contenuDrug utilization studies
Ouvrir ce répertoire et afficher son contenuInternational Conference on Harmonization and the common technical document
Ouvrir ce répertoire et afficher son contenuKeynote address
Ouvrir ce répertoire et afficher son contenuGlobal and national efforts to reduce tobacco use
Ouvrir ce répertoire et afficher son contenuElectronic communication in the regulatory process
Ouvrir ce répertoire et afficher son contenuTransparency in monitoring the safety of medicines
Ouvrir ce répertoire et afficher son contenuPharmaceutical products for use in special groups
Ouvrir ce répertoire et afficher son contenuNeed for Bioequivalence
Ouvrir ce répertoire et afficher son contenuAntimicrobial resistance: battling the bugs
Ouvrir ce répertoire et afficher son contenuSafety issues of plasma-derived medicinal products
Ouvrir ce répertoire et afficher son contenuHerbal medicines
Ouvrir ce répertoire et afficher son contenuRegulation and access to essential drugs
Afficher le documentParticipants
Afficher le documentBack cover
 

Counterfeit drugs: challenges and solutions

Moderators: Dr G. Vecina Neto, Brazil, and Dr H. Rees, South Africa

There is widespread recognition that, at its worse, counterfeiting can lead to significant morbidity and mortality. This is particularly serious with regard to the high percentage of counterfeit antibiotics and steroids available. The amount of counterfeit drugs increases in developing countries - the possibility of counterfeits being offered in the United Kingdom is less than i%, and in Brazil it is less than 5% - while in Niger it is 40%. Unfortunately, there is a general lack of national data available on counterfeit drugs.

At the national level, there is a need to encourage increased reporting of possible counterfeit drugs. A basis for suspicion of counterfeiting and reporting would be different appearance of drug or packaging from the original, ineffective action, or very low price. At the national and international levels, industry should be more closely engaged in identifying possible counterfeit medicine outlets.

Many countries should focus attention on the appearance of counterfeit drugs on the domestic market. Equally important is the regulation of exports. Maintaining the standards of exporting companies must be seen as an integral role of legislation and regulation. The need for improved international cooperation is essential through organizations such as WHO, UNICEF and Interpol.

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Dernière mise à jour: le 3 mai 2013