Counterfeit Drugs
(1999; 61 pages) [French] [Spanish] View the PDF document
Table of Contents
View the documentExecutive Summary
Open this folder and view contents1. Introduction
View the document2. Overview of the problem
View the document3. Impact on public health
View the document4. Factors facilitating counterfeiting
Open this folder and view contents5. Developing national strategies
Close this folder6. Specific measures
View the document6.1 Strengthening political will and commitment
View the document6.2 Promulgating appropriate legislation
View the document6.3 Establishing a national drug regulatory authority
View the document6.4 Developing standard operating procedures and guidelines for drug inspectors
View the document6.5 Enforcing drug control laws
View the document6.6 Empowering the judiciary
View the document6.7 Fostering partnerships
View the document6.8 Sharing responsibilities
Open this folder and view contents7. Assessment of the problem at the national level
Open this folder and view contents8. Inspection when pharmaceutical products are suspected to be counterfeit, spurious or substandard
Open this folder and view contents9. Test methods
Open this folder and view contents10. Developing training programmes: inspection and examination of counterfeit pharmaceuticals
View the document11. Conclusion
View the documentReferences
View the documentSelected further reading
View the documentAcknowledgements
View the documentGlossary
 

6.6 Empowering the judiciary

Countries should regard the counterfeiting of drugs as a serious offence and their judiciary should be empowered to impose harsh sentences in keeping with the nature of the contravention. Many calls have been made for the imposition of very severe penalties.

Counterfeiting cases should be given priority and handled speedily in the court system, and the courts should be empowered to order the confiscation, forfeiture and destruction of any detected counterfeit drugs.

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Last updated: May 3, 2013