Please use this identifier to cite or link to this item: http://repo.jfn.ac.lk/med/handle/701/1814
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dc.contributor.authorKarbwang, Juntra-
dc.contributor.authorKoonrungsesomboon, Nut-
dc.contributor.authorMuhunthan, K.-
dc.date.accessioned2018-11-09T03:34:27Z-
dc.date.accessioned2022-09-16T11:04:36Z-
dc.date.available2018-11-09T03:34:27Z-
dc.date.available2022-09-16T11:04:36Z-
dc.date.issued2018-
dc.identifier.citationBMC Medical Ethics (2018) 19:79en_US
dc.identifier.urihttp://repo.jfn.ac.lk/med/handle/701/1814-
dc.language.isoenen_US
dc.publisherBioMed Centralen_US
dc.subjectConsent formsen_US
dc.subjectInformed consenten_US
dc.subjectDisclosureen_US
dc.subjectInformationen_US
dc.subjectEthicsen_US
dc.subjectResearch subjectsen_US
dc.titleWhat information and the extent of information research participants need in informed consent forms: a multi-country surveyen_US
dc.typeJournal full texten_US
Appears in Collections:Gynecology & Obstetrics

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