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Appendix B: Background Discussion Document: Selected Guidelines for Transparent Reporting
Pages 105-110

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From page 105...
... guidelines;1 the National Academies of Sciences, Engineering, and Medicine report on Reproducibility and Replicability in Science;2 and the National Institutes of Health (NIH) policy on Enhancing Reproducibility through Rigor and Transparency.3 Each of the guidelines summarized below has a different scope and purpose.
From page 106...
... checklist for authors represents a generic set of minimum require ments applicable to all reporting studies in the life sciences for the explicit purpose of increasing transparent reporting and reproduc ibility, developed by the MDAR working group specifically seek ing common reporting points from across multiple journals. The checklist is being pilot tested by volunteer journals, and therefore has not been published at the time of this writing.
From page 107...
... • The Preferred Reporting Items for Systematic Reviews and Meta Analyses (PRISMA) statement recommends an evidence-based minimum set of reporting elements for systematic reviews and meta-analyses; was developed by an international group; and was first published in 2009 in multiple journals (PLOS Medicine, Annals of Internal Medicine, BMJ, Journal of Clinical Epidemiology, and Open Medicine)
From page 108...
... 1. NIH policies represented include Data Sharing Policy, Dissemination of NIH-Funded Clinical Trial Information, and Rigor and Transparency.
From page 109...
... 5. Covered by multiple NIH policies and offices, including Human Subjects Research policies and the NIH Office of Laboratory Animal Welfare.


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