Wiley develops AI guidelines in response to demand from researchers
Find out more about the guidelines aiming to embrace use of AI, ethically.
A central online news resource for professionals involved in the development of medical publications and involved in publication planning and medical writing.
Find out more about the guidelines aiming to embrace use of AI, ethically.
A recent survey sheds light on publisher perspectives on plain language summaries and the barriers to their wider adoption.
Discover the RIGHT-COI&F checklist, developed to improve conflict of interest and funding reporting in healthcare guidelines.
Find out how publisher AI policies need to evolve in the face of fast-changing technology.
Planning to write an overview of systematic reviews? Uncover essential guidance on the effective use of tools to assess and minimise bias.
All you need to know about the latest updates to the ICMJE recommendations.
How to improve outcome reporting in clinical trial protocols: read more about the SPIRIT-Outcomes 2022 Extension.
The 17 items to include when reporting clinical trial outcomes. Read about the CONSORT-Outcomes 2022 Extension checklist for outcomes of all randomised clinical trials.
Read about new guidance from the PMCPA that aims to ensure the social media activities of pharmaceutical companies stay within the law.
Find out what’s new in the latest 2022 update to the ICMJE recommendations.
Find out what’s covered in the 2022 update to the Good Publication Practice guidelines.
Read about the new 28-item checklist developed to aid decision-making in health economic evaluations.
Read about recent roundtable recommendations for improving the transparency of real world evidence dissemination.
Recommendations from the ISMPP Authorship Task Force aim to clarify ICMJE guidelines on authorship selection criteria.
Dr Tony Ross-Hellauer (ON-MERRITT) discusses how the move toward open research may exacerbate inequity and suggests strategies to prevent it.
Read about Cochrane reviewers’ approaches to detecting and tackling potential fraud in clinical trial publications.