To ensure the research that we published is conducted in an ethical manner, especially the research that involving human subject or animal participants, we require that all submissions should conform to the high ethical standards. We reserve the rights to reject any manuscript which could not meet these requirements of ethical standards, even if authors have obtained ethical approval or if ethical approval is not required.
1) Research involving human subjects
Ethical Approval
For published research based on human subjects (human participants, human tissue, human material or human data), authors must obtain the approval from institutional ethics committee(s) prior to the commencement of the research. The research also need to conform to international ethical and legal standards for research.
Authors should provide evidence that they obtained ethical and/or legal approval prior to conducting the research at submission. Manuscripts should include the name of the local ethics committee that approved the research (or confirmation that such approval is not needed) and the approval number. Authors also need to state how the study conforms to recognized standards (e.g. declaration of Helsinki or the Ethical Review Methods for Biomedical Research involving Humans) in the manuscript.
- Example of the statement: “The research was conducted in accordance with the Declaration of Helsinki, and the protocol was approved by the Ethics Committee of XXX (the approval number).”
2) Participant/patient privacy and informed consent
Published research involving human subjects should ensure that patients’ privacy has not been infringed without prior consent:
Consent to participate
For all published research involving human participants, authors should obtain written consent from the participants prior to the commencement of the research. If the research participants are not adults, or unable to provide informed consent, the written consent must be given from their parents/guardians.
Where consent for participation was not obtained or only verbal informed consent obtained, the journal/editor might ask for the evidence of consent or consent procedures, or even the need for consent was waived by an ethics committee.
Consent to publish
For submissions that include any information which might identify an individual, authors should obtain written informed consent to publish from individual participants (or their parents/guardians if the participant is not an adult or unable to give informed consent). Identifying information includes (but is not limited to) photographs, videos, individual clinical data, written description and any other details that might identify the participant. A statement to confirm that consent to publish has been obtained must be included within the manuscript.
3) Research involving animals, specimens and heritage sites
Research involving animals
For published research involving animal research, authors must obtain the approval from the relevant institutional ethics committee prior to the commencement of the research. The research procedures must comply with relevant local and international animal welfare guidelines.
Authors should provide evidence that they obtained ethical and/or legal approval prior to conducting the research at submission. Manuscripts should include the name of the ethics committee and the approval number.
Research involving specimens
For published research involving the collection of biological specimens (cultivated or wild), samples or fossils, authors should carry out it follow the authors’ institution(s) guideline and national/international regulations. Authors should also comply with the local laws. All such samples must be collected in an ethical and equitable way, and in accordance with relevant applicable laws comply with local legislation, and the manuscript should include a statement of appropriate permissions granted and/or licenses.
The manuscript should include the Ethical Statement of appropriate permissions granted. Voucher specimens must be deposited in an accessible herbarium or other public collection providing access to deposited material. Information on the voucher specimen and who identified it must be included in the manuscript. Editors reserve the rights to reject any manuscript which could not meet these requirements.
4) Clinical trials registration
All clinical trials should make prospective registration in publicly accessible databases (e.g., ClinicalTrials.gov) before participants are enrolled. The clinical trials also need to follow the CONSORT (CONsolidated Standards of Reporting Trials) guideline. Manuscripts should include clinical registration name, registration identification number, the name of the register, and the URL for the registry in accordance with journal instructions.