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Volumn 322, Issue 7296, 2001, Pages 1199-
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Registries will have to apply for right to collect patients’ data without consent
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Author keywords
[No Author keywords available]
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Indexed keywords
ARTICLE;
CONFIDENTIALITY;
FACTUAL DATABASE;
HEALTH CARE AND PUBLIC HEALTH;
HUMAN;
LEGAL APPROACH;
LEGAL ASPECT;
PATIENT ADVOCACY;
PUBLIC HEALTH;
REGISTER;
STATISTICS;
UNITED KINGDOM;
HEALTH CARE AND PUBLIC HEALTH;
LEGAL APPROACH;
CONFIDENTIALITY;
DATABASES, FACTUAL;
GREAT BRITAIN;
HUMANS;
PATIENT ADVOCACY;
PUBLIC HEALTH;
REGISTRIES;
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EID: 18044403937
PISSN: 09598138
EISSN: None
Source Type: Journal
DOI: 10.1136/bmj.322.7296.1199 Document Type: Article |
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Times cited : (9)
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References (0)
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