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 The Agreement on Technical Barriers to Trade (TBT)

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The Agreement on Technical Barriers to Trade (TBT) - Globalisation and the Impact on Health - A Third World View - Issue Papers

Globalisation and the Impact on Health
A Third World View - The Agreement on Technical Barriers to Trade (TBT)

 
This complete document inThis document in pdf formatpdf format 458 kb
 
Evelyne Hong

August 2000 
 

References
Conclusion
Socio Economic Causes of Ill Health
The Asian Financial Crisis
The US-UN Sanctions on Iraq
The Culture of Violence
The Globalisation of Culture
The Agreement on Agriculture (AOA)
The General Agreement on Trade in Services (GATS)
The Agreement on Trade Related Aspects of Intellectual Property (TRIPs)
The Agreement on Technical Barriers to Trade (TBT)
The Agreement on the Application of Sanitary and Phytosanitary Measures (SPS)
The World Trade Organisation (WTO)
The Role of the World Bank
The Global Assault on Health
Impact of SAPs in the Third World
Structural Adjustment Programmes (SAPs)
The Role of the World Bank in Global Economic Reform
Free Market Rules
Free Market Reform
Post-Colonial Development Strategy
Integration into the Market
The Colonial Enterprise
Introduction

 
 
 
The Agreement on Technical Barriers to Trade (TBT)
 

The TBT Agreement also has a bearing on the production, labelling, packaging and quality standards of pharmaceuticals, biologicals, foodstuffs and other technology assessments (Koivusalo 1999). It deals with various aspects of food labelling, and with claims relating to health and nutrition, which are made for food products. The Agreement also covers other health related commodities, medicinal products and medical devices.

The TBT Agreement encourages member states to apply internationally agreed standards as a basis for their technical regulations, but unlike the SPS Agreement it does not identify them. As the TBT covers a very broad range of products, the Agreement does not specify the international standards to be taken as a reference. Should a trade dispute arise involving biologicals, the dispute settlement panel might have to take a decision on which standards should apply to that case. They could be WHO’s guidelines and requirements for good manufacturing practices for biological substances (e.g. vaccines and blood products) or the norms of another standardizing body. This will bring on uncertainty as to what might happen in a dispute e.g. like vaccines; for which manufacturers have differing, yet equally valid standards. It might raise the issue of whether to apply WHO’s standard or those of industry, both of which are recognised under the TBT Agreement (Kinnon 1998). These concerns have far reaching implications for health.
  

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