about
Data Safe Havens in health research and healthcareVariation in recruitment across sites in a consent-based clinical data registry: lessons from the Canadian Stroke NetworkAlternatives to project-specific consent for access to personal information for health research: what is the opinion of the Canadian public?Guidelines for confidentiality and cancer registration.
P2860
description
article publié dans la revue scientifique British Medical Journal
@fr
im März 2001 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published in the British Medical Journal
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в березні 2001
@uk
name
Rights involve responsibilities for patients
@en
Rights involve responsibilities for patients
@nl
type
label
Rights involve responsibilities for patients
@en
Rights involve responsibilities for patients
@nl
prefLabel
Rights involve responsibilities for patients
@en
Rights involve responsibilities for patients
@nl
P1433
P1476
Rights involve responsibilities for patients
@en
P407
P577
2001-03-24T00:00:00Z