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Correction: Medicines and Healthcare products Regulatory Agency’s “Consultation on proposals for legislative changes for clinical trials”: a response from the Trials Methodology Research Partnership Adaptive Designs Working Group, with a focus on data sharing
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664262/ https://www.ncbi.nlm.nih.gov/pubmed/37990330 http://dx.doi.org/10.1186/s13063-023-07763-6 |
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author | Law, Martin Couturier, Dominique-Laurent Choodari-Oskooei, Babak Crout, Phillip Gamble, Carrol Jacko, Peter Pallmann, Philip Pilling, Mark Robertson, David S. Robling, Michael Sydes, Matthew R. Villar, Sofía S. Wason, James Wheeler, Graham Williamson, S. Faye Yap, Christina Jaki, Thomas |
author_facet | Law, Martin Couturier, Dominique-Laurent Choodari-Oskooei, Babak Crout, Phillip Gamble, Carrol Jacko, Peter Pallmann, Philip Pilling, Mark Robertson, David S. Robling, Michael Sydes, Matthew R. Villar, Sofía S. Wason, James Wheeler, Graham Williamson, S. Faye Yap, Christina Jaki, Thomas |
author_sort | Law, Martin |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-10664262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106642622023-11-21 Correction: Medicines and Healthcare products Regulatory Agency’s “Consultation on proposals for legislative changes for clinical trials”: a response from the Trials Methodology Research Partnership Adaptive Designs Working Group, with a focus on data sharing Law, Martin Couturier, Dominique-Laurent Choodari-Oskooei, Babak Crout, Phillip Gamble, Carrol Jacko, Peter Pallmann, Philip Pilling, Mark Robertson, David S. Robling, Michael Sydes, Matthew R. Villar, Sofía S. Wason, James Wheeler, Graham Williamson, S. Faye Yap, Christina Jaki, Thomas Trials Correction BioMed Central 2023-11-21 /pmc/articles/PMC10664262/ /pubmed/37990330 http://dx.doi.org/10.1186/s13063-023-07763-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Correction Law, Martin Couturier, Dominique-Laurent Choodari-Oskooei, Babak Crout, Phillip Gamble, Carrol Jacko, Peter Pallmann, Philip Pilling, Mark Robertson, David S. Robling, Michael Sydes, Matthew R. Villar, Sofía S. Wason, James Wheeler, Graham Williamson, S. Faye Yap, Christina Jaki, Thomas Correction: Medicines and Healthcare products Regulatory Agency’s “Consultation on proposals for legislative changes for clinical trials”: a response from the Trials Methodology Research Partnership Adaptive Designs Working Group, with a focus on data sharing |
title | Correction: Medicines and Healthcare products Regulatory Agency’s “Consultation on proposals for legislative changes for clinical trials”: a response from the Trials Methodology Research Partnership Adaptive Designs Working Group, with a focus on data sharing |
title_full | Correction: Medicines and Healthcare products Regulatory Agency’s “Consultation on proposals for legislative changes for clinical trials”: a response from the Trials Methodology Research Partnership Adaptive Designs Working Group, with a focus on data sharing |
title_fullStr | Correction: Medicines and Healthcare products Regulatory Agency’s “Consultation on proposals for legislative changes for clinical trials”: a response from the Trials Methodology Research Partnership Adaptive Designs Working Group, with a focus on data sharing |
title_full_unstemmed | Correction: Medicines and Healthcare products Regulatory Agency’s “Consultation on proposals for legislative changes for clinical trials”: a response from the Trials Methodology Research Partnership Adaptive Designs Working Group, with a focus on data sharing |
title_short | Correction: Medicines and Healthcare products Regulatory Agency’s “Consultation on proposals for legislative changes for clinical trials”: a response from the Trials Methodology Research Partnership Adaptive Designs Working Group, with a focus on data sharing |
title_sort | correction: medicines and healthcare products regulatory agency’s “consultation on proposals for legislative changes for clinical trials”: a response from the trials methodology research partnership adaptive designs working group, with a focus on data sharing |
topic | Correction |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664262/ https://www.ncbi.nlm.nih.gov/pubmed/37990330 http://dx.doi.org/10.1186/s13063-023-07763-6 |
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