Reporting Standards Of GPP

Good publication practise can develop to ensure that pharmaceutical companies' clinical trials are published responsibly and ethically. The main Principle of Good Publication Practice is the design, and the results of all the trials should report in a perfect, precise, balanced, unambiguous, and timely manner. The guidelines on the GPP can evolve to give the editors and journals a framework to help them deal with the range of multiple ethical issues that arise in scientific publishing. Evolving standards for the accurate publication and research presentation
Type of guideline/principles/ publications   Name
Randomized trial CONSORT (Consolidated Standards Of Reporting Trials)
Observational studies STROBE (Strengthening the Reporting of Observational Studies in Epidemiology)
Systematic review and meta-analysis PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses)
Studies of diagnostic accuracy STARD (Standards for Reporting of Diagnostic Accuracy)
Economic evaluations of health interventions CHEERS statement (Consolidated Health Economic Evaluation Reporting Standards)
For completeness, transparency and data analysis in case reports, and data from the point of care CARE (Case Reports)
Reporting of qualitative research studies SRQR (Standards for Reporting Qualitative Research)
Code of ethics and position statement: the contribution of medical writers to scientific publications AMWA (American Medical Writers Association)
Multiple resources for editors COPE (Committee on Publication Ethics)
White Paper on publication ethics CSE (Council of Science Editors)
Guidelines on the role of medical writers in developing peer-reviewed publications EMWA (European Medical Writers Association)
PERK (Publishing Ethics Resource Kit) Elsevier
Conflicts of interest in biomedical research—the FASEB guidelines FASEB (Federation of American Societies for Experimental Biology)
Recommendations for the conduct, reporting, editing, and publication of ICMJE (International Committee of Medical Journal Editors)
Code of ethics and position statement: the contribution of medical writers to scientific publications ISMPP (International Society for Medical Publication Professionals)
Pharmacoeconomic guidelines around the world ISPOR (International Society for Pharmacoeconomics and Outcomes Research)
Report on conflict of interest in medical research, education, and practice IOM (Institute of Medicine)
Principles on the conduct of clinical trials and communication of clinical trial results PhRMA (Pharmaceutical Research and Manufacturers of America)
World Association of Medical Editors policy statements prepared by the editorial policy committee WAME (World Association of Medical Editors)
Best practice guidelines on publication ethics: A publisher’s perspective Wiley publisher

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