Data protection legislation: interpretation and barriers to research.
about
Strategies designed to help healthcare professionals to recruit participants to research studiesStrategies to increase participant recruitment to research studies by healthcare professionalsA systematic review of barriers to data sharing in public healthPublic responses to the sharing and linkage of health data for research purposes: a systematic review and thematic synthesis of qualitative studiesSharing patient data: competing demands of privacy, trust and research in primary careThe new NHS information technology strategy. Technology will change practiceThe Domesday dataset: linked open data in disability studies.Data protection and patients' consent. Informed consent should be sought before data are used by registries.The Data Protection Act (1998): implications for health researchers.The Data Protection Act 1998: an audit of its effect on surgical trainees' practice.Clinical databases and data protection: are they compatible?Public attitudes towards the use of primary care patient record data in medical research without consent: a qualitative study.Using patient-identifiable data for epidemiological research.Patient/family views on data sharing in rare diseases: study in the European LeukoTreat project.Consent, confidentiality, and the Data Protection Act.Legal and ethical considerations in processing patient-identifiable data without patient consent: lessons learnt from developing a disease register.Community attitudes to the collection and use of identifiable data for health research--is it an invasion of privacy?A cost-effectiveness analysis of subject recruitment strategies in the HIPAA era: results from a colorectal cancer screening adherence trial.Cancer registries fear collapse. Need for patient consent for cancer registration creates logistical nightmareThe use of routinely collected patient data for research: a critical review.Supporting ethical practice in primary care research: strategies for action.Ethical review of health service research in the UK: implications for nursing.Legal aspects of records based medical researchObstacles to conducting epidemiological research in the UK general population.Experiences of the BMJ ethics committee.GMC's guidance may inhibit research.Are consenters representative of a target population?Guidelines for confidentiality and cancer registration.
P2860
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P2860
Data protection legislation: interpretation and barriers to research.
description
2000 nî lūn-bûn
@nan
2000 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Data protection legislation: interpretation and barriers to research.
@ast
Data protection legislation: interpretation and barriers to research.
@en
type
label
Data protection legislation: interpretation and barriers to research.
@ast
Data protection legislation: interpretation and barriers to research.
@en
prefLabel
Data protection legislation: interpretation and barriers to research.
@ast
Data protection legislation: interpretation and barriers to research.
@en
P2860
P356
P1433
P1476
Data protection legislation: interpretation and barriers to research.
@en
P2093
P2860
P304
P356
10.1136/BMJ.321.7265.890
P407
P50
P577
2000-10-01T00:00:00Z