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Author Instructions

           ClinicalTrials.gov. The trial registration number should be listed at the end of the Abstract section.
           Secondary data analyses of primary (parent) clinical trials should not be registered as a new clinical trial, but rather
           reference the trial registration number of the primary trial.
           Editors of RDODJ will consider carefully whether studies failed to register or had an incomplete trial registration. Because
           of the importance of prospective trial registration, if there is an exception to this policy, trials must be registered and the
           authors should indicate in the publication when registration was completed and why it was delayed. Editors will publish
           a statement indicating why an exception was allowed. Please note such exceptions should be rare, and authors failing to
           prospectively register a trial risk its inadmissibility to RDODJ.
           Authors who are not sure whether they need trial registration may refer to ICMJE FAQs for further information.
           3.2 Research Involving Animals
           Experimental  research  on  animals  should  be  approved  by  an  appropriate  ethics  committee  and  must  comply  with
           institutional, national, or international guidelines. RDODJ encourages authors to comply with the AALAS Guidelines,
           the ARRIVE Guidelines, and/or the ICLAS Guidelines, and obtain prior approval from the relevant ethics committee.
           Manuscripts must include a statement indicating that the study has been approved by the relevant ethical committee and the
           whole research process complies with ethical guidelines. If a study is granted an exemption from requiring ethics approval,
           the name of the ethics committee granting the exemption and the reason(s) for the exemption should be detailed. Editors
           will take account of animal welfare issues and reserve the right to reject a manuscript, especially if the research involves
           protocols that are inconsistent with commonly accepted norms of animal research.
           3.3 Research Involving Cell Lines
           Authors must describe what cell lines are used and their origin so that the research can be reproduced. For established cell
           lines, the provenance should be stated and references must also be given to either a published paper or to a commercial
           source. For de novo cell lines derived from human tissue, appropriate approval from an institutional review board or
           equivalent ethical committee, and consent from the donor or next of kin, should be obtained. Such statements should be
           listed on the Declaration section of Ethical Approval and Consent to Participate in the manuscript.
           Further information is available from the International Cell Line Authentication Committee (ICLAC). RDODJ recommends
           that authors check the NCBI database for misidentification and contamination of human cell lines.


           3.4 Research Involving Plants
           Experimental  research  on  plants  (either  cultivated  or  wild),  including  collection  of  plant  material,  must  comply  with
           institutional, national, or international guidelines. Field studies should be conducted in accordance with local legislation,
           and the manuscript should include a statement specifying the appropriate permissions and/or licenses. RDODJ recommends
           that authors comply with the IUCN Policy Statement on Research Involving Species at Risk of Extinction and the Convention
           on the Trade in Endangered Species of Wild Fauna and Flora.
           For each submitted manuscript, supporting genetic information and origin must be provided for plants that were utilized. For
           research manuscripts involving rare and non-model plants (other than, e.g., Arabidopsis thaliana, Nicotiana benthamiana,
           Oriza sativa, or many other typical model plants), voucher specimens must be deposited in a public herbarium or other
           public collections providing access to deposited materials.

           3.5 Publication Ethics Statement
           OAE is a member of the Committee on Publication Ethics (COPE). We fully adhere to its Code of Conduct and to its Best
           Practice Guidelines.
           The  Editors  of  RDODJ  enforce  a  rigorous  peer-review  process  together  with  strict  ethical  policies  and  standards  to
           guarantee to add high-quality scientific works to the field of scholarly publication. Unfortunately, cases of plagiarism, data
           falsification, image manipulation, inappropriate authorship credit, and the like, do arise. The Editors of RDODJ take such
           publishing ethics issues very seriously and are trained to proceed in such cases with zero tolerance policy.
           Authors wishing to publish their papers in RDODJ must abide to the following:
           The author(s) must disclose any possibility of a conflict of interest in the paper prior to submission.
           The authors should declare that there is no academic misconduct in their manuscript in the cover letter.
           Authors should accurately present their research findings and include an objective discussion of the significance of their
           findings.
           Data and methods used in the research need to be presented in sufficient detail in the manuscript so that other researchers
           can replicate the work.
           Authors should provide raw data if referees and the Editors of the journal request.
           Simultaneous submission of manuscripts to more than one journal is not tolerated.
           Republishing content that is not novel is not tolerated (for example, an English translation of a paper that is already published
           in another language will not be accepted).
           The manuscript should not contain any information that has already been published. If you include already published
                 Rare Disease and Orphan Drugs Journal                                                    XI
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