How common is data sharing for COVID-19 preprints?
An analysis of early COVID-19 preprints identified low uptake of data sharing statements and making data accessible.
How to lower the carbon footprint of clinical and biomedical research?
Learn about proposed strategies to make clinical trials more environmentally friendly and reduce biomedical research waste.
Are we still missing the mark with randomised controlled trial abstracts?
Adherence to the Consolidated Standards of Reporting Trials for Abstracts continues to be inadequate, nearly 15 years after their release.
Addressing race and ethnicity in medical literature
Learn about the current failings in race and ethnicity reporting in regulatory documents and medical literature and how they can be overcome.
CHEERS 2022 statement: reporting guidance for health economic evaluations gets a makeover
Read about the new 28-item checklist developed to aid decision-making in health economic evaluations.
[VIDEO]: Writing for Patients: Who, What, Where, When, Why and How?
Medical Communications and Patient Recruitment team members from IQVIA discuss life writing for lay audiences in this webinar.
GPP 2022: latest guidelines for company-sponsored publications are out now
Find out what’s new in the eagerly awaited 2022 update to the Good Publication Practice guidelines published in August.
What can be done to increase the transparency of real world studies?
Read about recent roundtable recommendations for improving the transparency of real world evidence dissemination.
[PODCAST] Privacy matters: protecting data amid evolving laws and technology
Jordan Fischer describes how privacy laws may impact medical publication professionals.
[VIDEO] ISMPP Authorship Algorithm Tool
Watch this ISMPP U webinar to find out more about the Authorship Algorithm Tool.
ISMPP West 2022 – Take The Lead: Learning. Engagement. Application. Development
ISMPP West 2022 will be held on September 26-27, 2022, in Irvine, California, USA. Register now!
GRReaT expectations: are editable templates the future of manuscript writing?
Read about EQUATOR Network’s updated GoodReports website, new downloadable and editable article templates and a call for researchers to help test whether the templates improve research reporting.
What counts as a ‘substantial contribution’ to industry-sponsored research?
Recommendations from the ISMPP Authorship Task Force aim to clarify ICMJE guidelines on authorship selection criteria.
New STROBE-MR guideline lights the way for Mendelian randomisation studies
Find out what’s in the new STROBE-MR checklist for reporting of observational epidemiology studies using Mendelian randomisation.
Are ‘living’ literature reviews the future of guideline development?
Discover ‘living’ evidence synthesis as a way to develop clinical practice guidelines that keep up to date with rapidly emerging new data.
Considering sex and gender in medical research: insights from the lead author of the SAGER guidelines
Read Shirin Heidari’s thoughts on the importance of incorporating sex and gender dimensions in clinical research design and reporting.