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11/10/2016 Recommendations to improve adverse event reporting in clinical trial publications: a joint pharmaceutical industry/journal editor perspective 10/02/2016 PRISMA harms checklist: improving harms reporting in systematic reviews 21/06/2013 Anecdotes as evidence 20/06/2013 Recommendations for reporting adverse drug reactions and adverse events of traditional Chinese medicine 20/06/2013 Guidelines for submitting adverse event reports for publication

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  • Why did we develop TIDieR-Placebo?

    The TIDieR reporting guideline helps authors fully report their interventions, so that they can be used by others. However, TIDieR only explicitly covers active interventions, not placebo controls. The developers of the new TIDieR-Placebo extension explain why it is needed Read More