Streamlining Technical Measured on Medical Products to Combat COVID-19
The urgency of effective responses to the COVID-19 pandemic and the reliance of many low-income countries on imports of medical products, requires new approaches to regulation of these products. The challenge will be particularly acute for the new...
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2020
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okr-10986-338252021-05-25T09:56:34Z Streamlining Technical Measured on Medical Products to Combat COVID-19 Jensen, Michael Friis Sela, Shane Brenton, Paul Keyser, John CORONAVIRUS COVID-19 MEDICAL GOODS TRADE NON-TARIFF MEASURES INTERNATIONAL STANDARD TECHNICAL TRADE BARRIER TRADE REGULATION CUSTOMS INSPECTION PRODUCT REGULATION MEDICAL PRODUCT PANDEMIC RESPONSE The urgency of effective responses to the COVID-19 pandemic and the reliance of many low-income countries on imports of medical products, requires new approaches to regulation of these products. The challenge will be particularly acute for the new tests to identify infection, drugs to alleviate symptoms and machines to aid recovery as well as vaccines that are all expected to be developed in the coming months. Increased transparency, information sharing and greater cooperation among agencies responsible for the approval and inspection of medical goods around the world can help officials in low-income countries implement their mandate more effectively while maximizing efficient access to these commodities. Responsible agencies should focus on implementing technical regulations to protect health and safety, including interception of counterfeit and substandard products, and avoid wasting resources and creating delays by maintaining procedural practices that may be better addressed through alternative risk management strategies or seeking to regulate quality issues, which are best left to the market. Where there is a need to rapidly approve, test and inspect new goods or varieties that have not previously been imported, such as new equipment and medicines, the adoption of mutual recognition and/or equivalence can provide effective mechanisms to avoid regulatory delays while maintaining high levels of safety. 2020-05-29T15:35:21Z 2020-05-29T15:35:21Z 2020-05-21 Policy Note http://documents.worldbank.org/curated/en/304931590509092851/Streamlining-Technical-Measured-on-Medical-Products-to-Combat-COVID-19 http://hdl.handle.net/10986/33825 English Trade and COVID-19 Guidance Note; CC BY 3.0 IGO http://creativecommons.org/licenses/by/3.0/igo World Bank World Bank, Washington, DC Economic & Sector Work Economic & Sector Work :: Policy Note |
repository_type |
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Foreign Institution |
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Digital Repositories |
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World Bank Open Knowledge Repository |
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World Bank |
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English |
topic |
CORONAVIRUS COVID-19 MEDICAL GOODS TRADE NON-TARIFF MEASURES INTERNATIONAL STANDARD TECHNICAL TRADE BARRIER TRADE REGULATION CUSTOMS INSPECTION PRODUCT REGULATION MEDICAL PRODUCT PANDEMIC RESPONSE |
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CORONAVIRUS COVID-19 MEDICAL GOODS TRADE NON-TARIFF MEASURES INTERNATIONAL STANDARD TECHNICAL TRADE BARRIER TRADE REGULATION CUSTOMS INSPECTION PRODUCT REGULATION MEDICAL PRODUCT PANDEMIC RESPONSE Jensen, Michael Friis Sela, Shane Brenton, Paul Keyser, John Streamlining Technical Measured on Medical Products to Combat COVID-19 |
relation |
Trade and COVID-19 Guidance Note; |
description |
The urgency of effective responses to
the COVID-19 pandemic and the reliance of many low-income
countries on imports of medical products, requires new
approaches to regulation of these products. The challenge
will be particularly acute for the new tests to identify
infection, drugs to alleviate symptoms and machines to aid
recovery as well as vaccines that are all expected to be
developed in the coming months. Increased transparency,
information sharing and greater cooperation among agencies
responsible for the approval and inspection of medical goods
around the world can help officials in low-income countries
implement their mandate more effectively while maximizing
efficient access to these commodities. Responsible agencies
should focus on implementing technical regulations to
protect health and safety, including interception of
counterfeit and substandard products, and avoid wasting
resources and creating delays by maintaining procedural
practices that may be better addressed through alternative
risk management strategies or seeking to regulate quality
issues, which are best left to the market. Where there is a
need to rapidly approve, test and inspect new goods or
varieties that have not previously been imported, such as
new equipment and medicines, the adoption of mutual
recognition and/or equivalence can provide effective
mechanisms to avoid regulatory delays while maintaining high
levels of safety. |
format |
Policy Note |
author |
Jensen, Michael Friis Sela, Shane Brenton, Paul Keyser, John |
author_facet |
Jensen, Michael Friis Sela, Shane Brenton, Paul Keyser, John |
author_sort |
Jensen, Michael Friis |
title |
Streamlining Technical Measured on Medical Products to Combat COVID-19 |
title_short |
Streamlining Technical Measured on Medical Products to Combat COVID-19 |
title_full |
Streamlining Technical Measured on Medical Products to Combat COVID-19 |
title_fullStr |
Streamlining Technical Measured on Medical Products to Combat COVID-19 |
title_full_unstemmed |
Streamlining Technical Measured on Medical Products to Combat COVID-19 |
title_sort |
streamlining technical measured on medical products to combat covid-19 |
publisher |
World Bank, Washington, DC |
publishDate |
2020 |
url |
http://documents.worldbank.org/curated/en/304931590509092851/Streamlining-Technical-Measured-on-Medical-Products-to-Combat-COVID-19 http://hdl.handle.net/10986/33825 |
_version_ |
1764479596793692160 |