Low risk research using routinely collected identifiable health information without informed consent: encounters with the Patient Information Advisory Group-Reference-Cited by-同舟云学术

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Low risk research using routinely collected identifiable health information without informed consent: encounters with the Patient Information Advisory Group

Published:2008-01-01 Issue:1 Volume:34 Page:37-40
ISSN:0306-6800
Container-title:Journal of Medical Ethics
language:en
Short-container-title:Journal of Medical Ethics

Author:

Metcalfe C,Martin R M,Noble S,Lane J A,Hamdy F C,Neal D E,Donovan J L

Publisher

BMJ

Subject

Health Policy,Arts and Humanities (miscellaneous),Issues, ethics and legal aspects,Health (social science)

Cited by 22 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Considerations for an integrated population health databank in Africa: lessons from global best practices;Wellcome Open Research;2021-08-23

2. Student and Staff Perspectives on the Use of Big Data in the Tertiary Education Sector: A Scoping Review and Reflection on the Ethical Issues;Review of Educational Research;2020-09-23

3. Active monitoring, radical prostatectomy and radical radiotherapy in PSA-detected clinically localised prostate cancer: the ProtecT three-arm RCT;Health Technology Assessment;2020-08

4. “Let’s get the best quality research we can”: public awareness and acceptance of consent to use existing data in health research: a systematic review and qualitative study;BMC Medical Research Methodology;2013-06-04

5. Evaluation of a programme to increase referrals to stop-smoking services using Children's Centres and smoke-free families schemes;Addiction;2012-11-02

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