GeezerVisonThe World Wide Web, restored to 800 pixels of glory. |
| Home|About|Gaming cabinet|Archives|How it works|Starter sites |
GeezerVison is showing brill.com — Publishing Ethics & AI Policy
Jump to Content
Browse Our Titles
Publishing Ethics & AI Policy
In order to ensure the research integrity of our publications, and by so doing to ensure that we achieve our aim of providing scholars with superior service, Brill works closely with authors and editors to promote adherence to the core principles of publication ethics as articulated by the Committee on Publication Ethics (COPE). We encourage further exploration of COPE’s resources on their website. All manuscripts, archival materials, and supporting files (to include but not limited to interviews, images, data, infographics, audio and video, and facsimiles), whether submitted to a peer-reviewed publication (book series, journal, or major reference work) or a primary source online collection, are expected to conform to the standards of ethical behavior promulgated by COPE. For the benefit of our authors, editors, reviewers, readership, and staff, we have listed below the most pressing ethical concerns facing the academic publishing community. We encourage you to direct questions and concerns to [email protected]. For detailed discussion of and an abundance of resources to assist in handling specific cases of research misconduct and violations of publication ethics, please visit the COPE website. Read more: Download Brill’s Publication Ethics here: Brill’s Publication Ethics
Code of Conduct for EditorsDiversity, Equity, and Inclusion refer to efforts to create a more welcoming environment for all people and to foster more diverse, inclusive, and equitable communities. Brill is committed to advancing diversity, equity, and inclusion in academic communities we serve. We are collaborating closely with other publishers in this respect. This Code originates from those collaborations. In collaboration with Brill, the editors of journals and book series shall endeavour to promote diversity, equity, and inclusion in the editorial processes and policies, including, but not limited to, ensuring diversity, equity, and inclusivity within journals’ and book series’ editorial teams, reviewer pools, and authorship bases. Editors hold a position of power in the peer review process. They commission content, are responsible for rejections and reviewer selection, and have the final decision on what gets published in their journal or series. Therefore, editors have a pivotal role to play with respect to diversity, equity, and inclusion (DEI) within journal or book series processes. It is important that this responsibility is clearly set out to editors themselves and made publicly available to support accountability. Recommendations 1. Expectations regarding editors’ code of conduct in relation to DEI should be clearly set out, with their responsibilities, beyond quality, clearly defined. Some examples of the likely responsibilities of editors are listed below. We recognise that the role of editor varies among journals and book series, and so this list is not intended to be either prescriptive or exhaustive.
2. Editors shall evaluate manuscripts for their intellectual content without regard to race, gender, sexual orientation, religious belief, ethnic origin, or citizenship of the authors. 3. The editorial policies of the journal or series shall encourage transparency and complete, honest reporting, and the editor shall ensure that peer reviewers and authors have a clear understanding of what is expected of them. 4. When nominating potential editorial board members, the editor shall take account of the need for appropriate, inclusive, and diverse representation. When selecting editors, the editor-in-chief and the publisher should endeavour to ensure that the composition of the team is diverse in terms of both expertise and levels of seniority, with members providing balanced representation of different geographical regions, racial/ethnic groups, gender groups, various levels of seniority, and other groups. When selecting peer reviewers, editors should also endeavour to procure those from a diverse pool to ensure a balanced point of view. 5. Editors shall develop, with the guidance of the acquisitions editor, a thorough acquaintance with Brill’s Publication Ethics policy and procedures and shall abide by these in all matters related to the journal or book series and shall expect the same adherence of their editorial boards, authors, and peer reviewers. Brill’s Publication Ethics may be downloaded here. Questions and concerns related to publication ethics should be directed to [email protected]. Appeal For questions and appeal against editorial decisions, please contact the acquisitions editor of the journal or book series.
Publishing Ethics - Life Sciences PublicationsContents
Publication ethics and publication malpractice statement
Duties of the Publisher Peer review The factors that are taken into account in review are relevance, soundness, significance, originality, readability and language. The possible decisions include acceptance, acceptance with revisions, or rejection. If authors are encouraged to revise and resubmit a submission, there is no guarantee that the revised submission will be accepted. Rejected articles will not be re-reviewed. Commercial activities Plagiarism
Duties of Editors Publication decisions Fair play For a manuscript submitted by an author to a journal, who is also an editor of that journal, this editor may not be involved in the evaluation, peer review and decision process on that manuscript. Confidentiality Reviewers’ identities will not be disclosed. However, if reviewers wish to disclose their names, this is permitted. Disclosure and conflicts of interest Corrections Ensuring the integrity of the published record – suspected research or publication misconduct If serious concerns are raised by readers, reviewers, or others, about the conduct, validity, or reporting of academic work, the journal’s Management Team will initially contact the authors and allow them to respond to the concerns. If that response is unsatisfactory, it will be taken to the institutional level or other appropriate bodies. Once an investigation is concluded, comment will be published that explains the findings of the investigation. It may be decided to retract a paper if the Editorial Board is convinced that serious misconduct has happened. Retracted papers will be retained online, and they will be prominently marked as a retraction in all online versions, including the PDF, for the benefit of future readers.
Duties of Reviewers Contribution to editorial decisions Promptness Confidentiality Standards of objectivity Acknowledgement of sources Disclosure and conflict of interest
Duties of Authors Reporting standards Data access and retention Originality and plagiarism Multiple, redundant or concurrent publication Acknowledgement of sources Authorship of the paper The corresponding author should ensure that all appropriate co-authors and no inappropriate co-authors are included on the paper, and that all co-authors have seen and approved the final version of the paper and have agreed to its submission for publication. Use of Artificial Intelligence writing tools
Disclosure and conflicts of interest Fundamental errors in published works
Duties of Authors for studies involving animals or human subjects Ethical requirements for studies involving animal subjects Authors must mention the institutional, regional or national ethical approval committee, together with the registration number for the study. Studies involving animal subjects must meet the ethical guidelines (i.e. applicable to the institution, jurisdiction, etc., where the research was performed). Authors must demonstrate that experimental procedures conform to the accepted principles of animal welfare in experimental science. These principles are defined and explained in the European Convention for the Protection of Vertebrate Animals used for Experimental and Other Scientific Purposes and its appendix, or in the National Research Council Guide for the Care and Use of Laboratory Animals. If experimental methodology raises particular ethical or welfare concerns then the Editor can take additional guidance from Animals (Scientific Procedures) Act 1986, when making decisions. Ethical requirements for studies involving human subjects The authors must ensure that the identity of the subjects is not infringed by the information in the publication. Human subjects have a right to privacy that should not be violated without informed consent. Identifying information, including names, initials, or hospital numbers, should not be published in written descriptions, photographs, or pedigrees unless the information is essential for scientific purposes and the human subject (or parent or guardian) gives written informed consent for publication. Informed consent for this purpose requires that an identifiable human subject be shown the manuscript to be published. Medical studies on human subjects must follow the ethical principles of the Declaration of Helsinki (most recent revision), including adherence to the legal requirements of the study country. Ethical requirements for (medical) trials The publisher defines a clinical/medical trial based on the ICMJE guidelines as any research project that prospectively assigns people or a group of people to an intervention, with or without concurrent comparison or control groups, to study the relationship between a health-related intervention and a health outcome. Health-related interventions are those used to modify a biomedical or health-related outcome; examples include drugs, devices, behavioural treatments, educational programs, dietary interventions, quality improvement interventions, and process-of-care changes. Health outcomes are any biomedical or health-related measures obtained in patients or participants, including pharmacokinetic measures and adverse events. The publisher accepts publicly accessible registration in any registry that is a primary register of the WHO International Clinical Trials Registry Platform (ICTRP) that includes the 24-item trial registration data set or in ClinicalTrials.gov, which is a data provider to the WHO ICTRP. These registers are accessible to the public at no charge, open to all prospective registrants, managed by a not-for-profit organization, have a mechanism to ensure the validity of the registration data, and are electronically searchable. The purpose of clinical/medical trial registration is to prevent selective publication and selective reporting of research outcomes, to prevent unnecessary duplication of research effort, to help patients and the public know what trials are planned or ongoing into which they might want to enrol, and to help give ethics review boards considering approval of new studies a view of similar work and data relevant to the research they are considering. Retrospective registration, for example at the time of manuscript submission, meets none of these purposes. Those purposes apply also to research with alternative designs, for example observational studies.
Terms and Conditions | Privacy Statement | Cookie Settings | Accessibility | Legal Notice | Sitemap | Copyright © 2016-2026
Powered by PubFactory
|
| You are visitor 01402503 — GeezerVison does not store the pages you look up. Best viewed with Netscape Navigator 4.7 or Internet Explorer 6 at 800×600. No cookies required. |