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.The risk of re-identification versus the need to identify individuals in rare disease researchUsing personal health information in medical researchEthical issues in implementation research: a discussion of the problems in achieving informed consent.Legal and ethical considerations in processing patient-identifiable data without patient consent: lessons learnt from developing a disease register.Symptoms of post-concussional syndrome are non-specifically related to mild traumatic brain injury in UK Armed Forces personnel on return from deployment in Iraq: an analysis of self-reported data.The European data protection legislation and its consequences for public health monitoring: a plea for actionChallenges in evaluating Welfare to Work policy interventions: would an RCT design have been the answer to all our problems?A randomised controlled trial to compare opt-in and opt-out parental consent for childhood vaccine safety surveillance using data linkage: study protocol.Development and pilot of an internationally standardized measure of cardiovascular risk management in European primary care.The use of routinely collected patient data for research: a critical review.Evidence will help achieve consensus.Participant recruitment in sensitive surveys: a comparative trial of 'opt in' versus 'opt out' approachesA telephone survey of factors affecting willingness to participate in health research surveysA Randomised Controlled Trial of Consent Procedures for the Use of Residual Tissues for Medical Research: Preferences of and Implications for Patients, Research and Clinical Practice.50 ways to trace your veteran: increasing response rates can be cheap and effectiveAssessing and adjusting for non-response in the Millennium Cohort Family StudyBuilding application-related patient identifiers: what solution for a European country?Assessing the impact of the requirement for explicit consent in a hospital-based stroke study.Risk factors for post-traumatic stress disorder among UK Armed Forces personnel.Joint replacement recipients' views about health information privacy.Low risk research using routinely collected identifiable health information without informed consent: encounters with the Patient Information Advisory Group.Consent bias in research: how to avoid it.Perceptions of the impact a military career has on children.The risks of absolute medical confidentiality.The effect of seeking consent on the representativeness of patient cohorts: iron-deficiency anaemia and colorectal cancer.Whose interest? British newspaper reporting of use of medical records for research
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Consent, confidentiality, and the Data Protection Act.
@ast
Consent, confidentiality, and the Data Protection Act.
@en
type
label
Consent, confidentiality, and the Data Protection Act.
@ast
Consent, confidentiality, and the Data Protection Act.
@en
prefLabel
Consent, confidentiality, and the Data Protection Act.
@ast
Consent, confidentiality, and the Data Protection Act.
@en
P2860
P50
P921
P356
P1433
P1476
Consent, confidentiality, and the Data Protection Act.
@en
P2093
Amy Iversen
Kathleen Liddell
P2860
P304
P356
10.1136/BMJ.332.7534.165
P407
P577
2006-01-01T00:00:00Z