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. 2021 Oct 18;41(12):2826–2833. doi: 10.1038/s41372-021-01220-5

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© The Author(s) 2021

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/.

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Fig. 1 — The proportion of respondents from each stakeholder group is shown for the prompt that “preclinical research provides an assessment of safety that is adequate to proceed to conducting a drug study in neonates”. The responses by Neonatologists (n = 37) are shown in a blue line. The responses by Nurses (n = 130) are shown in an orange line. The responses by parents (n = 49) are shown in a grey line.