Publishers join with STM to develop new standardised tools to tackle paper mills.
Read about the new weapon in the fight against bogus scientific research articles.
Learn about the current failings in race and ethnicity reporting in regulatory documents and medical literature and how they can be overcome.
New study maps ties between the medical product industry and healthcare ecosystem, exposing regulatory and transparency issues.
World Health Organization provides 6 principles for regulation and governance of the technology.
European countries can’t agree on what counts as research misconduct, creating potential pitfalls for researchers.
Join the debate: learn about the potential benefits and risks of paying peer reviewers.
Find out how implementing key principles of evidence communication can help audiences make informed decisions on clinical research.
Combatting research integrity breaches: insights from Suzanne Farley, Director of the Springer Nature Research Integrity Group
Read Suzanne Farley’s perspectives on the steps one publisher is taking to address the growing problem of research misconduct.
A recent survey assessed the prevalence of editors altering peer review reports. Read about the results here.
Research integrity across the Atlantic: our summary of the first Biomedical Transparency Summit series webinar
Find out more about what was covered during the first 2021 webinar from the Center for Biomedical Research Transparency.
Find out how principles of research integrity can be put into practice to combat fraud and misconduct.
It is standard practice to name professional medical writers in publications, but how should we acknowledge subcontracted or freelance support?
Missed the meeting? Read our report on the symposium entitled “Research integrity & the medical communicator: what we do when no one is watching.”
Learn more about text recycling from the Text Recycling Research Project in this recent webinar hosted by COPE.
[VIDEO] Professional medical writing support and the quality, ethics and timeliness of clinical trial reporting: a systematic review
Obaro Evuarherhe, Principal Consultant at Oxford PharmaGenesis, discusses professional medical writing support and the quality, ethics and timeliness of clinical trial reporting.