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From The Embassy of Good Science
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|Has Link=https://www.ecfs.eu/sites/default/files/general-content-files/working-groups/ecfs-patient-registry/ECFSPR_CodeofConduct_1.1.pdf | |Has Link=https://www.ecfs.eu/sites/default/files/general-content-files/working-groups/ecfs-patient-registry/ECFSPR_CodeofConduct_1.1.pdf | ||
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|Involves=European Cystic Fibrosis Society | |Involves=European Cystic Fibrosis Society | ||
|Has Timepoint=2014 | |Has Timepoint=2014 | ||
|Has Location=Europe | |Has Location=Europe | ||
| + | |Has Virtue And Value=Confidentiality; Privacy | ||
| + | |Has Good Practice And Misconduct=Data Management; Conflicts of Interest | ||
| + | |Related To Research Area=LS - Life Sciences | ||
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Latest revision as of 20:56, 27 October 2020
ResourcesGuidelines
European Cystic Fibrosis Society (ECFS) Patient Registry Code of Conduct
What is this about?
The European Cystic Fibrosis Society is an international community of scientific and clinical professionals committed to improving survival and quality of life for people with cystic fibrosis by promoting high quality research, education and care.
Why is this important?
The ECFS Patient Registry collects demographic and clinical data from consenting people with cystic fibrosis in Europe. The information is used to deepen our understanding of cystic fibrosis, improve standards of care, and to facilitate public health planning. This code of conduct details the ways in which the registry should be used.
