The National Institutes of Health and guidance for reporting preclinical research

dc.contributor.authorMoher, David
dc.contributor.authorAvey, Marc
dc.contributor.authorAntes, Gerd
dc.contributor.authorAltman, Douglas G
dc.date.accessioned2015-11-23T15:41:27Z
dc.date.available2015-11-23T15:41:27Z
dc.date.issued2015-02-17
dc.date.updated2015-11-19T13:06:16Z
dc.description.abstractAbstract The quality of reporting clinical and preclinical research is not optimal. Reporting guidelines can help make reports of research more complete and transparent, thus increasing their value and making them more useful to all readers. Getting reporting guidelines into practice is complex and expensive, and involves several stakeholders, including prospective authors, peer reviewers, journal editors, guideline developers, and implementation scientists. Working together will help ensure their maximum uptake and penetration. We are all responsible for helping to ensure that all research is reported so completely that it is of value to everybody. Please see related article: http://dx.doi.org/10.1186/s12916-015-0266-y
dc.identifier.citationBMC Medicine. 2015 Feb 17;13(1):34
dc.identifier.urihttp://dx.doi.org/10.1186/s12916-015-0284-9
dc.identifier.urihttp://hdl.handle.net/10393/33304
dc.language.rfc3066en
dc.rights.holderMoher et al.; licensee BioMed Central.
dc.titleThe National Institutes of Health and guidance for reporting preclinical research
dc.typeJournal Article

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