about
"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.Cancer registries can provide evidence-based data to improve quality of care and prevent cancer deaths.National survey of British public's views on use of identifiable medical data by the National Cancer Registry.Community attitudes to the collection and use of identifiable data for health research--is it an invasion of privacy?Challenges in evaluating Welfare to Work policy interventions: would an RCT design have been the answer to all our problems?Saudi views on consenting for research on medical records and leftover tissue samples.Recruitment of representative samples for low incidence cancer populations: do registries deliver?Can current electronic systems meet drug safety and effectiveness requirements?Acceptability and perceived barriers and facilitators to creating a national research register to enable 'direct to patient' enrolment into research: the Scottish Health Research Register (SHARE).The bioethics of preterm labour.Can epidemiology clear the fog of war? Lessons from the 1990-91 Gulf War.Issues of patient consent: a study of paediatric high-dependency care.Clinical trials bureaucracy: unintended consequences of well-intentioned policy.Impact of privacy legislation on the number and characteristics of people who are recruited for research: a randomised controlled trial.Genetic research on rare familial disorders: consent and the blurred boundaries between clinical service and researchLow risk research using routinely collected identifiable health information without informed consent: encounters with the Patient Information Advisory Group.Randomized clinical trials: slow death by a thousand unnecessary policies?The effect of privacy legislation on observational research.Shouldn't patients decide who should access their records?Collecting and sharing information about harms.Guidelines for confidentiality and cancer registration.NHS national programme for information technology: programme erodes confidentiality of medical records.Data protection, informed consent, and research: Data Protection Act does not bar medical research.Data protection, informed consent, and research: Interpretation of legislation should reflect patients' views.The effect of consent guidelines on a multiple sclerosis register.The ethics of reflective research in single case study inquiryPerceptions of potential donors in the Swedish public towards information and consent procedures in relation to use of human tissue samples in biobanks: a population-based studyResearch governance: regulating risk and reducing harm?
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh-hant
name
Data protection, informed consent, and research.
@en
Data protection, informed consent, and research.
@nl
type
label
Data protection, informed consent, and research.
@en
Data protection, informed consent, and research.
@nl
prefLabel
Data protection, informed consent, and research.
@en
Data protection, informed consent, and research.
@nl
P1433
P1476
Data protection, informed consent, and research.
@en
P2093
Clare Gilham
P304
P356
10.1136/BMJ.328.7447.1029
P407
P577
2004-05-01T00:00:00Z