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23/09/2020 STrengthening the Reporting Of Pharmacogenetic Studies: Development of the STROPS guideline 28/11/2019 Guidelines for reporting case studies and series on drug-induced QT interval prolongation and its complications following acute overdose 26/07/2017 Guidance to develop individual dose recommendations for patients on chronic hemodialysis 11/10/2016 Recommendations to improve adverse event reporting in clinical trial publications: a joint pharmaceutical industry/journal editor perspective 20/04/2016 Developing the Clarity and Openness in Reporting: E3-based (CORE) reference user manual for creation of clinical study reports in the era of clinical trial transparency 11/03/2016 Reporting guidelines for population pharmacokinetic analyses 17/03/2015 Reporting Guidelines for Clinical Pharmacokinetic Studies: The ClinPK Statement 27/06/2013 Guidelines for field surveys of the quality of medicines: a proposal 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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