Literature DB >> 11230085

Data protection and patients' consent. Informed consent should be sought before data are used by registries.

J I Morrow.   

Abstract

Entities:  

Keywords:  Biomedical and Behavioral Research; General Medical Council (Great Britain)

Mesh：

Year:  2001        PMID： 11230085      PMCID： PMC1119743     

Source DB:  PubMed          Journal:  BMJ        ISSN： 0959-8138


× No keyword cloud information.
  3 in total

1.  Cancer registries fear imminent collapse.

Authors:  P Brown
Journal:  BMJ       Date:  2000-10-07

2.  Data protection legislation: interpretation and barriers to research.

Authors:  J Strobl; E Cave; T Walley
Journal:  BMJ       Date:  2000-10-07

3.  The computer research network of the Royal New Zealand College of General Practitioners: an approach to general practice research in New Zealand.

Authors:  S M Dovey; M W Tilyard
Journal:  Br J Gen Pract       Date:  1996-12       Impact factor: 5.386
  3 in total
  1 in total

1.  Legal and ethical considerations in processing patient-identifiable data without patient consent: lessons learnt from developing a disease register.

Authors:  Charlotte L Haynes; Gary A Cook; Michael A Jones
Journal:  J Med Ethics       Date:  2007-05       Impact factor: 2.903
  1 in total

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