ORCID is part of the wider digital infrastructure needed for researchers to share information on a global scale. ORCID enables transparent and trustworthy connections between researchers, their contributions, and affiliations by providing an identifier for individuals to use with their name as they engage in research, scholarship and innovation activities. The Open Pharma community is … Continue reading Guest post: ORCID adoption in the pharma community
Featuring researchers’ fears surrounding clinical trial registries, a roundup of the events planned for Open Access Week 2019 and the release of the Open Pharma Charter
Featuring the upcoming MedComms Brunch Meeting on open access, an investigation into the future of open access publishing, news from the third Asia Pacific Meeting of ISMPP and the scientific community’s toxic definition of success
Featuring the Open Pharma and Pint of Science crossover event, a new pilot project to facilitate the transparent review of preprints and the results from a Nature poll on coercive citations
Featuring a novel solution to prevent the spread of disreputable science, top tips on publication planning in small companies and editorial perspectives on the latest Plan S news
Featuring news from Peer Review Week, help for smaller scientific societies with the transition to Plan S and recommendations by NIH to make data more FAIR
Featuring the growing traction of Registered Reports, an investigation into the inconsistent role of a peer reviewer, unusual citation patterns in some manuscripts and a new Plan S toolkit
Featuring the pros and cons of ‘patient-orientated research’, a new addition to the Medical Publishing and Insights Practices (MPIP) open access toolkit and an update on Plan S.
Featuring concerns over financing ‘pay to publish’ models, a fresh demand for clinical trial transparency sanctions, and how one highly cited article may influence a journal’s impact factor and a researcher’s career progression.
Featuring the growing need for communication during each stage of the research process, the role of patient experts in a healthcare setting, the association of medical writing support with the quality of clinical trial reporting, and the replacement of supplementary material with online repositories.