Checklist
| | e. CONSORT (CONSOlidated standards of Reporting pragmatic Trials) | Full Record
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| | f. CONSORT (Statement to Randomized Trials of Non-pharmacologic Treatment) | Full Record
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| | g. CONSORT (Reporting randomized, controlled trials of herbal interventions) | Full Record
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| | h. CONSORT (Reporting of Harms in Randomized Trials) | Full Record
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| | i. CONSORT (CONSORT for Reporting Randomized Controlled Trials in Journal and Conference Abstracts) | Full Record
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| | j. CONSORT-PRO (CONSORT Patient-Reported Outcomes) | Full Record
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| | k. STRICTA (STandards for Reporting Interventions in Clinical Trials of Acupuncture) | Full Record
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| | l. RedHot (Reporting data on Homeopathic Treatments) | Full Record
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| | m. QUOROM (QUality Of Reporting Of Meta-analyses) | Full Record | Checklist
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| | n. MOOSE (Meta-analysis Of Observational Studies in Epidemiology) | Full Record | Checklist
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| | o. PRACTIHC (Pragmatic RAndomized Control TrIals in HealthCare) | Full Record
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| | p. REFLECT (Reporting guidElines For randomized controLled trials for livEstoCk and food safeTy) | Full Record
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| | r. FigCTR (Figures in Clinical Trial Reports) | Full Record
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| | s. SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) | Full Record | Checklist
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| 2 | a. STROBE (STrengthening the Reporting of OBservational studies in Epidemiology) | Full Record | Checklists
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| | b. STROBE-ME (STrengthening the Reporting of OBservational studies in Epidemiology – Molecular Epidemiology) | Full Record
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| | c. STROME-ID (STrengthening the Reporting of OBservational studies in Epidemiology for Infectious Diseases: | Full Record
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| | d. STRLOD-Rhe (STrengthening the Reporting of Longitudinal Observational Drug studies in Rheumatology Infectious Diseases: | Full Record | Checklist
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| | e. STRATOS (STRengthening Analytical Thinking for OBservational Studies) | Full Record
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| 3 | a. PRISMA (TransParent ReportIng of Systematic reviews and Meta-Analysis) | Full Record | Checklist | Flow Diagram
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| | b. PRISMA for Abstracts: | Full Record
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| | c. PRISMA-Equity 2012 Extension: | Full Record
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| | d. PRISMA-P (Preferred Reporting Items for Systematic review and Meta-Analysis Protocols (PRISMA-P) 2015 statement) | Full Record
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| 4 | PROGRESS (PROGnosis RESearch Strategy) | ROGRESS publications
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| | a. Research Clinical Outcomes | Full Record
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| | b. Prognostic Factor Research | Full Record
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| | c. Prognostic Model Research | Full Record
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| | d. Stratified Medicine Research | Full Record
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| | e. REMARK (Reporting REcommendations for Tumor MARKer prognostic studies) | Full Record
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| | f. ENMCR (criteria for Evaluation of Novel Markers of Cardiovascular Risk) | Full Record
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| 5 | a. GRIPS (Genetic RIsk Prediction Studies) | Full Record
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| | b. STREGA (STrengthening the REporting of Genetic Associations) | Full Record
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| 6 | a. STARD (STAndards for Reporting of Diagnostic accuracy) | Full Record | Checklist | Flow Diagram
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| | b. STARDem (STAndards for Reporting of Diagnostic accuracy in demetia) | Full Record - Cochrane Dementia and Cognitive Improvement Group | Checklist | Flow Diagram
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| | c. GRCMRE (Guidelines for Reporting Cardiovascular Magnetic Resonance Examinations) | Full Record - Cochrane Dementia and Cognitive Improvement Group
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| | d. MIfMRI (Minimum Information about an fMRI Study) | Full Record
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| | e. QUADAS-2 (QUality Assessment of Diagnostic Accuracy Studies) | Full Record & QUADAS-2
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| 7 | a. COREQ (COnsolidated criteria for REporting Qualitative research) | Full Record
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| | b. ENTREQ (ENhancing Transparency in REporting the synthesis of Qualitative research) | Full Record
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| 8 | a. ARRIVE (Animal Research: Reporting of InVivo Experiments) | Full Record | Checklist
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| | b. CAMARADES (Collaborative Approach to Meta-Analysis and Review of Animal Data from Experimental Studies) | Full Record
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| | c. PGRPR (Principles and Guidelines for Reporting Preclinical Research) | Full record
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| 9 | a. CHEERS (Consolidated Health Economic Evaluation Reporting Standards) | Full Record
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| | b. STARE-HI (STAtement on REporting of evaluation studies in Health Informatics) | Full Record
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| | c. CARE (consensus-based Clinical cAse REporting guideline) | Full Record | Checklist
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| 10 | a. TIDieR (Template for Intervention Description and Replication) | Full Record | Checklist
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| | b. CLIP (Documenting Clinical and Laboratory Images in Publications) | Full Record
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| | c. MIBBI (Minimum Information for Biological and Biomedical Investigations) | Full Record
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| | d. MIAME (Minimum Information About a Microarray Experiment) | Full Record
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| | e. SQUIRE (Standards for QUality Improvement Reporting Excellence) | Full Record | Checklist
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| | f. ORION (Outbreak Reports and Intervention studies Of Nosocomial infection) | Full Record | Checklist
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| | g. SDTM (Study Data Tabulation Model) | Full Record
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| 11 | a. CDASH (Clinical Data Acquisition Standards Harmonization) | Full Record
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| | b. GLP (Good Laboratory Practice: preventing introduction of bias at the bench) | Abstract
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| | c. SEND (Standard for Exchange of Nonclinical Data) | Full Record
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| | d. AST (Authors' Submission Toolkit) | Full Record
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| 12 | a. GPP2 (Good Publication Practice) | Full Record
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| | b. SAMPL (Statistical Analyses and Methods in the Published Literature) | Full Record
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| | c. SBE-PIsCT (BPSPharmaceutical Industry-sponsored Clinical Trials) | Full Record
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| | d. R-MLogR (Reporting of Multivariable Logistic Regression) | Full Record
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| | e. SACT (reporting of Subgroup Analyses in Clinical Trials) | Full Record
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| | e. PRDP (Preparing Raw clinical Data for Publication) | Full Record
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| 13 | a. PCE (Professionals Code of Ethics) | Full Record
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| | b. CBCSP (Contributions of Biomedical Communicators to Scientific Publications) | Full Record
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| | c. EMWA-MeR (European Medical Writers Association guidelines on the role of Medical Writers in developing peer-reviewed publications) | Full Record
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| | d. FCI-CR (Financial Conflicts of Interest for Clinical Research studies) | Full Record
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| | e. HGWPSJ (How to Get your Writing Published in Scholarly Journals, by Linda Olson) | Full Record
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| 14 | QRF (Qualitative Research in Feasibility studies for trials | Full Record
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