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Open Access

Peer-reviewed

Research Article

Informed consent and trial prioritization for clinical studies during the COVID-19 pandemic. Stakeholder experiences and viewpoints

Stefanie Weigold,

Roles Data curation, Formal analysis, Investigation, Project administration, Writing – original draft

Affiliation QUEST Center for Responsible Research, Berlin Institute of Health (BIH) at Charité – Universitätsmedizin Berlin, Berlin, Germany
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Susanne Gabriele Schorr,

Roles Formal analysis, Project administration, Writing – review & editing

Affiliation QUEST Center for Responsible Research, Berlin Institute of Health (BIH) at Charité – Universitätsmedizin Berlin, Berlin, Germany
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Alice Faust,

Roles Formal analysis, Investigation, Writing – review & editing

Affiliation QUEST Center for Responsible Research, Berlin Institute of Health (BIH) at Charité – Universitätsmedizin Berlin, Berlin, Germany
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Lena Woydack,

Roles Data curation, Formal analysis, Investigation, Project administration, Writing – original draft

Affiliation QUEST Center for Responsible Research, Berlin Institute of Health (BIH) at Charité – Universitätsmedizin Berlin, Berlin, Germany
⨯
Daniel Strech

Roles Conceptualization, Supervision, Validation, Writing – original draft

* E-mail: daniel.strech@bih-charite.de

Affiliation QUEST Center for Responsible Research, Berlin Institute of Health (BIH) at Charité – Universitätsmedizin Berlin, Berlin, Germany

https://orcid.org/0000-0002-9153-079X

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Informed consent and trial prioritization for clinical studies during the COVID-19 pandemic. Stakeholder experiences and viewpoints

Stefanie Weigold,
Susanne Gabriele Schorr,
Alice Faust,
Lena Woydack,
Daniel Strech

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Published: April 30, 2024
https://doi.org/10.1371/journal.pone.0302755

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27 Jun 2024
16:06 GMT
Most Recent

Funding statement Update Posted by PLOS_ONE_Group on 27 Jun 2024 at 16:06 GMT

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