Proceedings of the Ninth International Conference of Drug Regulatory Authorities (ICDRA) - Berlin, Germany 25-29 April 1999
(1999; 102 pages) View the PDF document
Table of Contents
Open this folder and view contentsOpening Ceremony
Open this folder and view contentsGood regulatory practice
Open this folder and view contentsGood certification practice
Close this folderCounterfeit drugs: challenges and solutions
View the documentIllicit pharmaceutical markets
View the documentThe situation of counterfeit drugs
View the documentRecommendations
Open this folder and view contentsCurrent issues in regulation and quality
Open this folder and view contentsInternational Conference on Harmonization: implementation and implications
Open this folder and view contentsDrug utilization studies
Open this folder and view contentsInternational Conference on Harmonization and the common technical document
Open this folder and view contentsKeynote address
Open this folder and view contentsGlobal and national efforts to reduce tobacco use
Open this folder and view contentsElectronic communication in the regulatory process
Open this folder and view contentsTransparency in monitoring the safety of medicines
Open this folder and view contentsPharmaceutical products for use in special groups
Open this folder and view contentsNeed for Bioequivalence
Open this folder and view contentsAntimicrobial resistance: battling the bugs
Open this folder and view contentsSafety issues of plasma-derived medicinal products
Open this folder and view contentsHerbal medicines
Open this folder and view contentsRegulation and access to essential drugs
View the documentParticipants
View the 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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Last updated: April 24, 2012