Proceedings of the Tenth International Conference of Drug Regulatory Authorities (ICDRA) - Hong Kong, China, 24 - 27 June 2002
(2002; 166 pages) Ver el documento en el formato PDF
Índice de contenido
Ver el documentoAbbreviations and acronyms used in this report
Abrir esta carpeta y ver su contenidoOpening ceremony
Abrir esta carpeta y ver su contenidoHerbal medicines
Abrir esta carpeta y ver su contenidoKeynote address
Abrir esta carpeta y ver su contenidoSafety of blood-derived products
Abrir esta carpeta y ver su contenidoAntimicrobial resistance - new initiatives
Abrir esta carpeta y ver su contenidoHarmonization I
Abrir esta carpeta y ver su contenidoHarmonization II
Abrir esta carpeta y ver su contenidoProtection of trial subjects in clinical trials
Abrir esta carpeta y ver su contenidoRegulating biotechnology products
Abrir esta carpeta y ver su contenidoRegulatory challenges: health sector reform and drug regulatory capacity
Abrir esta carpeta y ver su contenidoAccess to drugs and vaccines I
Cerrar esta carpetaAccess to drugs and vaccines II
Ver el documentoTwenty-five years of essential medicines: progress and agenda for regulators
Ver el documentoEssential drugs list: South African experience
Ver el documentoThe role of government and essential drugs - Indonesian experience
Ver el documentoThailand’s experience in access to medicines
Ver el documentoCurrent vaccine shortages in the United States of America
Ver el documentoExpanding access to essential medicines and vaccines: lessons learnt in Brazil
Ver el documentoRecommendations
Abrir esta carpeta y ver su contenidoCounterfeit pharmaceutical products
Abrir esta carpeta y ver su contenidoHomoeopathy
Abrir esta carpeta y ver su contenidoSafety monitoring
Abrir esta carpeta y ver su contenidoE-Commerce
Abrir esta carpeta y ver su contenidoCurrent topics
Abrir esta carpeta y ver su contenidoRegulatory challenges of new technologies
Ver el documentoList of participants
Ver el documentoBack cover
 

Recommendations

1. Countries should implement programmes aimed at assuring the availability, accessibility, quality and rational use of essential medicines.

2. The Model List of Essential Medicines is a central element of national drug policies. WHO should continue to maintain the Model List and support countries in adapting it to their needs and national context. Selection of essential medicines should be based on safety, quality and efficacy in addition to accessibility.

3. Access to medicines is improved by competition brought about by generic products. Countries should take measures to foster the development of a competitive generic market.

4. Countries and WHO should further develop initiatives aimed at expanding the implementation of the concept of essential medicines to encompass both the public and private sectors.

5. Countries and WHO should intensify efforts aimed at improving access to vital medicines, particularly those used for HIV/AIDSrelated care and treatment.

6. Problems of vaccine availability are becoming more frequent. Countries and WHO should intensify their efforts to prevent supply shortages.

7. Countries and WHO should continue to study the impact of international trade agreements on access to medicines and initiatives aimed at promoting essential medicines and rational use.

8. Progress should be reported back to the ICDRA

 

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Última actualización: le 3 mayo 2013