Proceedings of the Eighth International Conference of Drug Regulatory Authorities (ICDRA) - Bahrain, 10-13 November 1996
(1996; 111 pages) View the PDF document
Table of Contents
Open this folder and view contentsOpening ceremony
Open this folder and view contentsInternational harmonization of regulatory requirements Plenary: 10 November 1996
Open this folder and view contentsGlobal harmonization
Open this folder and view contentsTripartite harmonization - International Conference on Harmonization (ICH)
Open this folder and view contentsRegional harmonization activities
Open this folder and view contentsAgreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS)
Open this folder and view contentsThe mission of drug regulatory authorities
Close this folderCounterfeit drugs
View the documentCombating counterfeiters - Dr K. Jones, United Kingdom
View the documentCounterfeit medicines: a special case for concern - Margaret Cone, IFPMA
View the documentCountry studies on counterfeit drugs - Mr Eshetu Wondemagegnehu, DAP/WHO
View the documentWHO guidelines to combat counterfeit drugs - Professor T. Paal, Hungary
View the documentRapid detection of counterfeit drags using simple tests - Dr S. Mizuno, Japan
View the documentWHO data base on counterfeit medicines - Dr K. Kimura, WHO
View the documentRecommendations
Open this folder and view contentsComputer-assisted drug registration
Open this folder and view contentsUpdates
Open this folder and view contentsThe challenge of biotechnology
Open this folder and view contentsPharmacovigilance
Open this folder and view contentsWHO Certification scheme: current developments
Open this folder and view contentsRegulatory control and assessment of herbal medicines
Open this folder and view contentsRegistration requirements for multisource products (generics)
View the documentList of participants
 

WHO data base on counterfeit medicines - Dr K. Kimura, WHO

In response to a request by the World Health Assembly, WHO's Division of Drug Management & Policies and the Drug Action Programme have established a joint programme to prevent and detect counterfeit pharmaceutical products. One of the activities of this programme has been the establishment in 1992 of a data base to serve Member States in their efforts to combat this practice internationally. Sources of the material in the data base differ but the majority of the material comes from regulatory authorities, professional associations, manufacturers, nongovernmental organizations and articles in the published literature.

The number of reports which WHO has compiled varies each year, but it is encouraging to note that the number is increasing rapidly. For reasons of security, reports must remain confidential, but they are of considerable value in providing statistical information and orienting authorities and interested parties to the kind of products which will be targeted by counterfeiters. As shown below, the majority of detected counterfeit products are also a country's best selling medicines.


Pharmacotherapeutic classes of cases

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Last updated: May 3, 2013