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A brief introduction to institutional review boards in the United States
China has become one of the main fields for international drug and device trials in the last twenty years. Although China has greatly strengthened the protection of human research participants over this time, there is still room for improvement. In order for Chinese investigators to participate in i...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331443/ https://www.ncbi.nlm.nih.gov/pubmed/32851230 http://dx.doi.org/10.1002/ped4.12023 |
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author | Qiao, Haiping |
author_facet | Qiao, Haiping |
author_sort | Qiao, Haiping |
collection | PubMed |
description | China has become one of the main fields for international drug and device trials in the last twenty years. Although China has greatly strengthened the protection of human research participants over this time, there is still room for improvement. In order for Chinese investigators to participate in international clinical trials, compliance with internationally recognized ethical regulations is essential. In the United States (U.S.), research involving human subjects is reviewed by an ethics committee called the Institutional Review Board (IRB). In this article, we briefly introduce the background, composition, and function of the IRB in the U.S. to our Chinese investigators. |
format | Online Article Text |
id | pubmed-7331443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73314432020-08-25 A brief introduction to institutional review boards in the United States Qiao, Haiping Pediatr Investig Lecture China has become one of the main fields for international drug and device trials in the last twenty years. Although China has greatly strengthened the protection of human research participants over this time, there is still room for improvement. In order for Chinese investigators to participate in international clinical trials, compliance with internationally recognized ethical regulations is essential. In the United States (U.S.), research involving human subjects is reviewed by an ethics committee called the Institutional Review Board (IRB). In this article, we briefly introduce the background, composition, and function of the IRB in the U.S. to our Chinese investigators. John Wiley and Sons Inc. 2018-05-11 /pmc/articles/PMC7331443/ /pubmed/32851230 http://dx.doi.org/10.1002/ped4.12023 Text en © 2018 Chinese Medical Association. Pediatric Investigation published by John Wiley & Sons Australia, Ltd on behalf of Futang Research Center of Pediatric Development. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Lecture Qiao, Haiping A brief introduction to institutional review boards in the United States |
title | A brief introduction to institutional review boards in the United States |
title_full | A brief introduction to institutional review boards in the United States |
title_fullStr | A brief introduction to institutional review boards in the United States |
title_full_unstemmed | A brief introduction to institutional review boards in the United States |
title_short | A brief introduction to institutional review boards in the United States |
title_sort | brief introduction to institutional review boards in the united states |
topic | Lecture |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331443/ https://www.ncbi.nlm.nih.gov/pubmed/32851230 http://dx.doi.org/10.1002/ped4.12023 |
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