Consent and the ethical duty to participate in health data research

Overview of attention for article published in Journal of Medical Ethics, January 2018

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In the top 5% of all research outputs scored by Altmetric
High Attention Score compared to outputs of the same age (95th percentile)
High Attention Score compared to outputs of the same age and source (87th percentile)

Mentioned by

blogs: 2 blogs
policy: 1 policy source

twitter: 41 X users

Readers on

mendeley: 130 Mendeley

So far, Altmetric has seen 43 X posts from 41 X users, with an upper bound of 104,002 followers.

Also, the impracticability requirement still applies to biomedical research governed by the Human Biomedical Research Act. But for an argument that impracticability is an unnecessary requirement when there's a strong public interest in the research, see…

ヘルスデータ研究への参加、同意と義務　Consent and the ethical duty to participate in health data research | Journal of Medical Ethics https://t.co/2HFJWXz709

RT @ECMontef: "Consent and the ethical duty to participate in health data research" https://t.co/jBPBnkvllY #bioethics #feedly

"Consent and the ethical duty to participate in health data research" https://t.co/jBPBnkvllY #bioethics #feedly

This page shows the most recent X posts that mention this research output. Click here to find out how to access more activity, including 39 additional X posts.