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Involvement of the European Medicines Agency in multi-stakeholder regulatory science research projects: experiences of staff members and project coordinators

BACKGROUND: The European Medicines Agency (EMA) interacts with many different stakeholders involved in the development of drugs, including academic researchers. In recent years, EMA has collaborated more closely with academia, inter alia by taking part in external research projects such as those set...

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Autores principales: Saesen, Robbe, Machado, Matilde, Crifo, Bianca, Liu, Lifang, de Vries, Corinne, Herold, Ralf, Llinares Garcia, Jordi, Huys, Isabelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267977/
https://www.ncbi.nlm.nih.gov/pubmed/37324145
http://dx.doi.org/10.3389/fmed.2023.1181702
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author Saesen, Robbe
Machado, Matilde
Crifo, Bianca
Liu, Lifang
de Vries, Corinne
Herold, Ralf
Llinares Garcia, Jordi
Huys, Isabelle
author_facet Saesen, Robbe
Machado, Matilde
Crifo, Bianca
Liu, Lifang
de Vries, Corinne
Herold, Ralf
Llinares Garcia, Jordi
Huys, Isabelle
author_sort Saesen, Robbe
collection PubMed
description BACKGROUND: The European Medicines Agency (EMA) interacts with many different stakeholders involved in the development of drugs, including academic researchers. In recent years, EMA has collaborated more closely with academia, inter alia by taking part in external research projects such as those set up under the Horizon 2020 program in general and the Innovative Medicines Initiative in particular. The aim of this study was to evaluate the perceived added value of EMA’s involvement in these projects, both from the perspective of the Agency’s participating Scientific Officers and of the coordinators of the consortia that undertook them. METHODS: Semi-structured interviews were conducted with the coordinators of 21 ongoing or recently finalized projects in which EMA has participated, as well as with the Agency experts contributing to them. RESULTS: In total, 40 individuals were interviewed, of whom 23 were project coordinators and 17 were EMA staff members. While most of the projects were reported to suffer from delays due to the SARS-CoV-2 pandemic, the consortia adapted to the circumstances and their members still expected to deliver on their objectives. EMA’s input into the projects ranged from providing guidance by reviewing documents and attending meetings to creating project materials and disseminating them. The frequency of communication between EMA and the consortia varied widely. The projects generated a diverse set of outputs, which encompassed new or improved medicinal products, methodological standards, research infrastructures, and educational tools. All of the coordinators expressed that EMA’s contributions to their projects had increased the scientific relevance of their consortium’s work, and the EMA experts found that the knowledge and the deliverables produced by the projects were valuable, taking into consideration the time they had invested into them. In addition, interviewees highlighted some actions which could be taken to increase the regulatory significance of the project outcomes. CONCLUSION: EMA’s engagement in external research projects benefits the consortia conducting them and supports the Agency’s mission to foster scientific excellence and advance regulatory science.
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spelling pubmed-102679772023-06-15 Involvement of the European Medicines Agency in multi-stakeholder regulatory science research projects: experiences of staff members and project coordinators Saesen, Robbe Machado, Matilde Crifo, Bianca Liu, Lifang de Vries, Corinne Herold, Ralf Llinares Garcia, Jordi Huys, Isabelle Front Med (Lausanne) Medicine BACKGROUND: The European Medicines Agency (EMA) interacts with many different stakeholders involved in the development of drugs, including academic researchers. In recent years, EMA has collaborated more closely with academia, inter alia by taking part in external research projects such as those set up under the Horizon 2020 program in general and the Innovative Medicines Initiative in particular. The aim of this study was to evaluate the perceived added value of EMA’s involvement in these projects, both from the perspective of the Agency’s participating Scientific Officers and of the coordinators of the consortia that undertook them. METHODS: Semi-structured interviews were conducted with the coordinators of 21 ongoing or recently finalized projects in which EMA has participated, as well as with the Agency experts contributing to them. RESULTS: In total, 40 individuals were interviewed, of whom 23 were project coordinators and 17 were EMA staff members. While most of the projects were reported to suffer from delays due to the SARS-CoV-2 pandemic, the consortia adapted to the circumstances and their members still expected to deliver on their objectives. EMA’s input into the projects ranged from providing guidance by reviewing documents and attending meetings to creating project materials and disseminating them. The frequency of communication between EMA and the consortia varied widely. The projects generated a diverse set of outputs, which encompassed new or improved medicinal products, methodological standards, research infrastructures, and educational tools. All of the coordinators expressed that EMA’s contributions to their projects had increased the scientific relevance of their consortium’s work, and the EMA experts found that the knowledge and the deliverables produced by the projects were valuable, taking into consideration the time they had invested into them. In addition, interviewees highlighted some actions which could be taken to increase the regulatory significance of the project outcomes. CONCLUSION: EMA’s engagement in external research projects benefits the consortia conducting them and supports the Agency’s mission to foster scientific excellence and advance regulatory science. Frontiers Media S.A. 2023-05-30 /pmc/articles/PMC10267977/ /pubmed/37324145 http://dx.doi.org/10.3389/fmed.2023.1181702 Text en Copyright © 2023 Saesen, Machado, Crifo, Liu, de Vries, Herold, Llinares Garcia and Huys. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Saesen, Robbe
Machado, Matilde
Crifo, Bianca
Liu, Lifang
de Vries, Corinne
Herold, Ralf
Llinares Garcia, Jordi
Huys, Isabelle
Involvement of the European Medicines Agency in multi-stakeholder regulatory science research projects: experiences of staff members and project coordinators
title Involvement of the European Medicines Agency in multi-stakeholder regulatory science research projects: experiences of staff members and project coordinators
title_full Involvement of the European Medicines Agency in multi-stakeholder regulatory science research projects: experiences of staff members and project coordinators
title_fullStr Involvement of the European Medicines Agency in multi-stakeholder regulatory science research projects: experiences of staff members and project coordinators
title_full_unstemmed Involvement of the European Medicines Agency in multi-stakeholder regulatory science research projects: experiences of staff members and project coordinators
title_short Involvement of the European Medicines Agency in multi-stakeholder regulatory science research projects: experiences of staff members and project coordinators
title_sort involvement of the european medicines agency in multi-stakeholder regulatory science research projects: experiences of staff members and project coordinators
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267977/
https://www.ncbi.nlm.nih.gov/pubmed/37324145
http://dx.doi.org/10.3389/fmed.2023.1181702
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