Responding to the Pandemic of Falsified Medicines
- Autores
- Nayyar, Gaurvika M. L.; Attaran, Amir; Clark, John P.; Culzoni, Maria Julia; Fernandez, Facundo M.; Herrington, James E.; Kendall, Megan; Newton, Paul N.; Breman, Joel G.
- Año de publicación
- 2015
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Over the past decade, the number of countries reporting falsified (fake, spurious/falsely labeled/counterfeit) medicines and the types and quantities of fraudulent drugs being distributed have increased greatly. The obstacles in combating falsified pharmaceuticals include 1) lack of consensus on definitions, 2) paucity of reliable and scalable technology to detect fakes before they reach patients, 3) poor global and national leadership and accountability systems for combating this scourge, and 4) deficient manufacturing and regulatory challenges, especially in China and India where fake products often originate. The major needs to improve the quality of the world?s medicines fall into three main areas: 1) research to develop and compare accurate and affordable tools to identify high-quality drugs at all levels of distribution; 2) an international convention and national legislation to facilitate production and utilization of high-quality drugs and protect all countries from the criminal and the negligent who make, distribute, and sell life-threatening products; and 3) a highly qualified, well-supported international science and public health organization that will establish standards, drug-quality surveillance, and training programs like the U.S. Food and Drug Administration. Such leadership would give authoritative guidance for countries in cooperation with national medical regulatory agencies, pharmaceutical companies, and international agencies, all of which have an urgent interest and investment in ensuring that patients throughout the world have access to good quality medicines. The organization would also advocate strongly for including targets for achieving good quality medicines in the United Nations Millennium Development Goals and Sustainable Development Goals.
Fil: Nayyar, Gaurvika M. L.. University Johns Hopkins; Estados Unidos
Fil: Attaran, Amir. University of Otawa; Canadá
Fil: Clark, John P.. Pfizer Pharmaceuticals; Estados Unidos
Fil: Culzoni, Maria Julia. Universidad Nacional del Litoral. Facultad de Bioquímica y Ciencias Biológicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe; Argentina
Fil: Fernandez, Facundo M.. University of North Carolina; Estados Unidos
Fil: Herrington, James E.. University of Otawa; Canadá
Fil: Kendall, Megan. Lao-Oxford-Mahosot Hospital; Reino Unido
Fil: Newton, Paul N.. University of Oxford; Reino Unido
Fil: Breman, Joel G.. National Institutes of Health; Estados Unidos - Materia
-
FALSIFIED MEDICINES
PANDEMIC
LABORATORY AND FIELD INNOVATIONS
POLICY PERSPECTIVES - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/46371
Ver los metadatos del registro completo
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Responding to the Pandemic of Falsified MedicinesNayyar, Gaurvika M. L.Attaran, AmirClark, John P.Culzoni, Maria JuliaFernandez, Facundo M.Herrington, James E.Kendall, MeganNewton, Paul N.Breman, Joel G.FALSIFIED MEDICINESPANDEMICLABORATORY AND FIELD INNOVATIONSPOLICY PERSPECTIVEShttps://purl.org/becyt/ford/3.3https://purl.org/becyt/ford/3Over the past decade, the number of countries reporting falsified (fake, spurious/falsely labeled/counterfeit) medicines and the types and quantities of fraudulent drugs being distributed have increased greatly. The obstacles in combating falsified pharmaceuticals include 1) lack of consensus on definitions, 2) paucity of reliable and scalable technology to detect fakes before they reach patients, 3) poor global and national leadership and accountability systems for combating this scourge, and 4) deficient manufacturing and regulatory challenges, especially in China and India where fake products often originate. The major needs to improve the quality of the world?s medicines fall into three main areas: 1) research to develop and compare accurate and affordable tools to identify high-quality drugs at all levels of distribution; 2) an international convention and national legislation to facilitate production and utilization of high-quality drugs and protect all countries from the criminal and the negligent who make, distribute, and sell life-threatening products; and 3) a highly qualified, well-supported international science and public health organization that will establish standards, drug-quality surveillance, and training programs like the U.S. Food and Drug Administration. Such leadership would give authoritative guidance for countries in cooperation with national medical regulatory agencies, pharmaceutical companies, and international agencies, all of which have an urgent interest and investment in ensuring that patients throughout the world have access to good quality medicines. The organization would also advocate strongly for including targets for achieving good quality medicines in the United Nations Millennium Development Goals and Sustainable Development Goals.Fil: Nayyar, Gaurvika M. L.. University Johns Hopkins; Estados UnidosFil: Attaran, Amir. University of Otawa; CanadáFil: Clark, John P.. Pfizer Pharmaceuticals; Estados UnidosFil: Culzoni, Maria Julia. Universidad Nacional del Litoral. Facultad de Bioquímica y Ciencias Biológicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe; ArgentinaFil: Fernandez, Facundo M.. University of North Carolina; Estados UnidosFil: Herrington, James E.. University of Otawa; CanadáFil: Kendall, Megan. Lao-Oxford-Mahosot Hospital; Reino UnidoFil: Newton, Paul N.. University of Oxford; Reino UnidoFil: Breman, Joel G.. National Institutes of Health; Estados UnidosAmerican Society of Tropical Medicine and Hygiene2015-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/46371Nayyar, Gaurvika M. L.; Attaran, Amir; Clark, John P.; Culzoni, Maria Julia; Fernandez, Facundo M.; et al.; Responding to the Pandemic of Falsified Medicines; American Society of Tropical Medicine and Hygiene; American Journal of Tropical Medicine and Hygiene; 92; suppl 6; 6-2015; 113-1180002-9637CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.4269/ajtmh.14-0393info:eu-repo/semantics/altIdentifier/url/http://www.ajtmh.org/content/journals/10.4269/ajtmh.14-0393info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T12:10:51Zoai:ri.conicet.gov.ar:11336/46371instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-22 12:10:51.695CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Responding to the Pandemic of Falsified Medicines |
| title |
Responding to the Pandemic of Falsified Medicines |
| spellingShingle |
Responding to the Pandemic of Falsified Medicines Nayyar, Gaurvika M. L. FALSIFIED MEDICINES PANDEMIC LABORATORY AND FIELD INNOVATIONS POLICY PERSPECTIVES |
| title_short |
Responding to the Pandemic of Falsified Medicines |
| title_full |
Responding to the Pandemic of Falsified Medicines |
| title_fullStr |
Responding to the Pandemic of Falsified Medicines |
| title_full_unstemmed |
Responding to the Pandemic of Falsified Medicines |
| title_sort |
Responding to the Pandemic of Falsified Medicines |
| dc.creator.none.fl_str_mv |
Nayyar, Gaurvika M. L. Attaran, Amir Clark, John P. Culzoni, Maria Julia Fernandez, Facundo M. Herrington, James E. Kendall, Megan Newton, Paul N. Breman, Joel G. |
| author |
Nayyar, Gaurvika M. L. |
| author_facet |
Nayyar, Gaurvika M. L. Attaran, Amir Clark, John P. Culzoni, Maria Julia Fernandez, Facundo M. Herrington, James E. Kendall, Megan Newton, Paul N. Breman, Joel G. |
| author_role |
author |
| author2 |
Attaran, Amir Clark, John P. Culzoni, Maria Julia Fernandez, Facundo M. Herrington, James E. Kendall, Megan Newton, Paul N. Breman, Joel G. |
| author2_role |
author author author author author author author author |
| dc.subject.none.fl_str_mv |
FALSIFIED MEDICINES PANDEMIC LABORATORY AND FIELD INNOVATIONS POLICY PERSPECTIVES |
| topic |
FALSIFIED MEDICINES PANDEMIC LABORATORY AND FIELD INNOVATIONS POLICY PERSPECTIVES |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.3 https://purl.org/becyt/ford/3 |
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Over the past decade, the number of countries reporting falsified (fake, spurious/falsely labeled/counterfeit) medicines and the types and quantities of fraudulent drugs being distributed have increased greatly. The obstacles in combating falsified pharmaceuticals include 1) lack of consensus on definitions, 2) paucity of reliable and scalable technology to detect fakes before they reach patients, 3) poor global and national leadership and accountability systems for combating this scourge, and 4) deficient manufacturing and regulatory challenges, especially in China and India where fake products often originate. The major needs to improve the quality of the world?s medicines fall into three main areas: 1) research to develop and compare accurate and affordable tools to identify high-quality drugs at all levels of distribution; 2) an international convention and national legislation to facilitate production and utilization of high-quality drugs and protect all countries from the criminal and the negligent who make, distribute, and sell life-threatening products; and 3) a highly qualified, well-supported international science and public health organization that will establish standards, drug-quality surveillance, and training programs like the U.S. Food and Drug Administration. Such leadership would give authoritative guidance for countries in cooperation with national medical regulatory agencies, pharmaceutical companies, and international agencies, all of which have an urgent interest and investment in ensuring that patients throughout the world have access to good quality medicines. The organization would also advocate strongly for including targets for achieving good quality medicines in the United Nations Millennium Development Goals and Sustainable Development Goals. Fil: Nayyar, Gaurvika M. L.. University Johns Hopkins; Estados Unidos Fil: Attaran, Amir. University of Otawa; Canadá Fil: Clark, John P.. Pfizer Pharmaceuticals; Estados Unidos Fil: Culzoni, Maria Julia. Universidad Nacional del Litoral. Facultad de Bioquímica y Ciencias Biológicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe; Argentina Fil: Fernandez, Facundo M.. University of North Carolina; Estados Unidos Fil: Herrington, James E.. University of Otawa; Canadá Fil: Kendall, Megan. Lao-Oxford-Mahosot Hospital; Reino Unido Fil: Newton, Paul N.. University of Oxford; Reino Unido Fil: Breman, Joel G.. National Institutes of Health; Estados Unidos |
| description |
Over the past decade, the number of countries reporting falsified (fake, spurious/falsely labeled/counterfeit) medicines and the types and quantities of fraudulent drugs being distributed have increased greatly. The obstacles in combating falsified pharmaceuticals include 1) lack of consensus on definitions, 2) paucity of reliable and scalable technology to detect fakes before they reach patients, 3) poor global and national leadership and accountability systems for combating this scourge, and 4) deficient manufacturing and regulatory challenges, especially in China and India where fake products often originate. The major needs to improve the quality of the world?s medicines fall into three main areas: 1) research to develop and compare accurate and affordable tools to identify high-quality drugs at all levels of distribution; 2) an international convention and national legislation to facilitate production and utilization of high-quality drugs and protect all countries from the criminal and the negligent who make, distribute, and sell life-threatening products; and 3) a highly qualified, well-supported international science and public health organization that will establish standards, drug-quality surveillance, and training programs like the U.S. Food and Drug Administration. Such leadership would give authoritative guidance for countries in cooperation with national medical regulatory agencies, pharmaceutical companies, and international agencies, all of which have an urgent interest and investment in ensuring that patients throughout the world have access to good quality medicines. The organization would also advocate strongly for including targets for achieving good quality medicines in the United Nations Millennium Development Goals and Sustainable Development Goals. |
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2015 |
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2015-06 |
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http://hdl.handle.net/11336/46371 Nayyar, Gaurvika M. L.; Attaran, Amir; Clark, John P.; Culzoni, Maria Julia; Fernandez, Facundo M.; et al.; Responding to the Pandemic of Falsified Medicines; American Society of Tropical Medicine and Hygiene; American Journal of Tropical Medicine and Hygiene; 92; suppl 6; 6-2015; 113-118 0002-9637 CONICET Digital CONICET |
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Nayyar, Gaurvika M. L.; Attaran, Amir; Clark, John P.; Culzoni, Maria Julia; Fernandez, Facundo M.; et al.; Responding to the Pandemic of Falsified Medicines; American Society of Tropical Medicine and Hygiene; American Journal of Tropical Medicine and Hygiene; 92; suppl 6; 6-2015; 113-118 0002-9637 CONICET Digital CONICET |
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