Clinical trials in neonates: How to optimise informed consent and decision making? A European Delphi survey of parent representatives and clinicians

• Virginia Neyro,

  Roles Methodology, Supervision, Writing – original draft, Writing – review & editing

  Affiliations Department of Paediatric Pharmacology and Pharmacogenetics, Assistance Publique des Hôpitaux de Paris, Robert Debré Hospital, Paris, France, Doctoral School MTCI – Paris Descartes University, Paris, France

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• Valéry Elie,

  Roles Methodology, Supervision, Writing – original draft, Writing – review & editing

  Affiliation Department of Paediatric Pharmacology and Pharmacogenetics, Assistance Publique des Hôpitaux de Paris, Robert Debré Hospital, Paris, France

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• Nicole Thiele,

  Roles Conceptualization, Writing – review & editing

  Affiliation European Foundation for the Care of Newborn Infants, EFCNI, Munich, Germany

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• Evelyne Jacqz-Aigrain

  Roles Conceptualization, Funding acquisition, Methodology, Resources, Supervision, Writing – review & editing

  * E-mail: evelyne.jacqz-aigrain@aphp.fr

  Affiliations Department of Paediatric Pharmacology and Pharmacogenetics, Assistance Publique des Hôpitaux de Paris, Robert Debré Hospital, Paris, France, INSERM Clinical Investigations Center CIC1426, Robert Debré Hospital, Paris, France, EA08 – Paris Diderot University, Paris, France

  http://orcid.org/0000-0002-4285-7067

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