The following are the standards of expected ethical behaviour for all parties involved in publishing in Journal of Chemical Health Risks: the author, the journal editor and editorial board, the peer reviewer and the publisher.
Duties of the editor and editorial board:
Duties of Reviewers:
Duties of Authors:
We required the authors to understand and accept the ethical policy especially:
Declaration of interests — it is important to declare the funding that made the research possible.
Registering clinical trials — clinical trials should be registered in publicly accessible registries.
Respecting confidentiality — protecting patients from being recognized if used in research and in publication.
Protecting research subjects, patients and experimental animals.
Ethics and consent
Every submission reporting a research must include a statement to verify that ethics approval was sought for the study (or a statement that it was not required and why), including the name of the ethics committee(s) or institutional review board(s), the reference number/ID of the approval(s), and a statement that participants gave informed consent before participating. Even when a study has been approved by a research ethics committee or institutional review board, editors may ask authors for more detailed information about the ethics of the work. Also, research involving human subjects, human tissue, or human data must have been performed in accordance with the declaration of
Allegations of publication misconduct, both before and after publication will be carefully inspected and we reserve the right to contact authors' institutions, funders, or regulatory bodies if necessary. If a conclusive evidence of misconduct is noticed, proper steps will be taken to correct the scientific record, which may include supplying a correction or retraction.
Authors are assumed that they are aware of publication ethics, specifically with regard to authorship, dual submission, plagiarism, figure manipulation, competing interests and compliance with standards of research ethics. In cases of suspected misconduct, COPE standards and practices will be followed and advice from the COPE forum will be ascertained.
Retrospective ethics approval
If a study has not been granted ethics committee approval prior to commencing, retrospective ethics approval usually cannot be obtained and it may not be possible to consider the submission for peer review. The decision on whether to proceed to peer review in such cases is at the discretion of the journals’ editors.
Patient consent and confidentiality
Any item submitted to the journals published by Damghan Branch, Islamic Azad University that contains personal medical information about an identifiable living individual requires patient’s explicit consent before it can be published. Consequently; all studied patients are required to sign an informed consent form after reading the studies’ information sheet.
If consent cannot be obtained because the patient cannot be traced in a study, then publication will be possible only if the information can be sufficiently anonymized. Anonymization means that neither the person nor anyone else could identify the individual with certainty.
If the patient is dead the authors should seek permission from a relative (as a matter of courtesy and medical ethics). If the relatives are not contactable, the journals will balance the worthwhileness of the case, the likelihood of identification, and the likelihood of offence in decision to publish a submitted paper.
Images—such as x-rays, laparoscopic images, ultrasound images, pathology slides, or images of undistinctive parts of the body—may be used without consent so long as they are anonymized by the removal of any identifying marks and are not accompanied by text that could reveal the patients’ identity.
Research involving animals
Experimental research on vertebrates or any regulated invertebrates must comply with institutional, national, or international guidelines, and where available should have been approved by an appropriate ethics committee. The Basel Declaration outlines fundamental principles to adhere when conducting research on animals and the International Council for Laboratory Animal Science (ICLAS) has also published ethical guidelines.
For experimental studies involving client-owned animals, authors must also document informed consent from the client or owner and adherence to a high standard (best practice) of veterinary care.
Based on the ICMJE recommendations a clinical trial is defined 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 cause-and-effect, relationship between a health-related intervention and a health outcome.”
In agreement with the ICMJE’s recommendations, all journals published by Damghan Branch, Islamic Azad University will not consider reports of clinical trials unless they were registered prospectively before recruitment of any participants.
As a condition of consideration for publication, journals published by the Damghan Branch, Islamic Azad University require registration of all trials in a public registry of trials approved by the ICMJE (any registry that is a primary register of the WHO International Clinical Trials Registry Platformwww.who.int/ictrp/network/primary/en/index.html).
The trial registration number and the date of registration should be included in the last line of the submission abstract.