publication . Book . 2021

Guidelines for Tailoring the Informed Consent Process in Clinical Studies

Diez-Domingo, Javier; Fons-Martínez, Jaime; García-Bayarri, Júlia; Calvo Rigual, Fernando; Petrova Dobreva, Dafina; Vázquez-Moreno, Mónica; Morales Cuenca, Valle; Ferrer-Albero, Cristina; Egea-Ferrer, Miguel; García Gómez, Alberto; ...
Open Access English
  • Published: 25 Mar 2021
  • Publisher: Zenodo
These guidelines have been designed to provide information and evidence to assist with the development, or review of the consent process for use in clinical studies with human participants. These guidelines do not deal with issues related to informed consent in clinical practice. The guidelines have been developed by the i-CONSENT consortium. i-CONSENT (H2020, Grant Agreement number 741856) is a European Union H2020 funded program that aims to improve the information that individuals receive when deciding whether or not to take part in clinical studies.
Medical Subject Headings: humanities
free text keywords: Informed consent, Ethics, Clinical research, H2020, Bioethics, Informed consent, Ethics, Clinical research, H2020, Bioethics
Funded by
Improving the guidelines for Informed Consent, including vulnerable populations, under a gender perspective
  • Funder: European Commission (EC)
  • Project Code: 741856
  • Funding stream: H2020 | CSA
Validated by funder
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Open Access
Book . 2021
Provider: Datacite
Open Access
Book . 2021
Provider: Datacite
Open Access
Book . 2021
Provider: ZENODO
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