Ethics in publishing

Termedia Publishing House is committed to upholding standards of ethical behaviour at all stages of the publication process. We follow closely the industry associations, such as the Committee on Publication Ethics (COPE), International Committee of Medical Journal Editors (ICJME) and World Association of Medical Editors (WAME), that set standards and provide guidelines for best practices in order to meet these requirements. Authors and editors, have ethical obligations with regard to the publication of the results of research. According to our publishing policy, manuscripts not conforming to the principles of the Declaration of Helsinki should not be accepted for publication.

DUTIES AND RESPONSIBILITIES OF AUTHORS
The Author(s) is obliged to prepare and send the article in accordance with the requirements set out in the journal Editor. Moreover the Author(s) is obliged to submit editorial complemented by a statement which will be included: a statement about the originality of the content of the article (work not yet published anywhere), the integrity of the copyrights of others, no conflict of interest or its application, as well as the superior permission to publish an article in the journal. Authors are obliged to participate in peer review process. The Author(s) are obliged to provide retractions or corrections of mistakes, they also should provide a list of references.
Author(s) are responsible for disclosing all financial and personal relationships that might bias or be seen to bias their work.
Authors may, at any time before accepting the article for publication, withdraw the article by submitting a statement in the electronic system of the Editorial System.

AUTHORSHIP CRITERIA AND/OR WHO SHOULD BE LISTED AS A CONTRIBUTOR
Termedia Publishing House in the matter of authorship criteria and/or who should be listed as a contributor, respects standards recommended by COPE (Committee on Publication Ethics). Detailed information about those criteria you can find in COPE Report publicationethics.org/files/2003pdf12_0.pdf.

POLICIES REGARDING PLAGIARISM
Plagiarism is using the words, tables, grafics or ideas of others and presenting them as your own. Such activity is a form of fraud. It can take many forms, from deliberately seeking academic advantage by replicating the work of others, to accidentally copying from a source without obtaining permission from the rights holder.
The Editor will not accept a paper which employs ghostwriting or guest authorship, and will disclose all such practices, especially symptoms of scientific dishonesty (breaking or compromising the ethical principles effective in scientific research) and plagiarism.
The author accepts that a submitted manuscript may be screened for plagiarism against previously published works (iThenticate - plagiarism checker). Manuscripts that are found to have been plagiarized will incur plagiarism sanctions: immediate rejection of the submitted manuscript or published article, prohibition of any new submissions.

POLICIES FOR RESEARCH ON HUMAN AND VULNERABLE POPULATIONS
Authors should follow the principles outlined in the Declaration of Helsinki of the World Medical Association (www.wma.net). The manuscript should contain a statement that the work has been approved by the relevant institutional review boards or ethics committees and that all human participants gave informed consent. Identifying information, including patients’ names, initials, or hospital numbers, should not be published.
Vulnerable populations (children) require special protection during research.Researchers need to consider additional ethics concerns or issues arising from working with potentially vulnerable persons. In cases where research involves potentially vulnerable groups, for example children, older persons or adults with learning disabilities, every effort should be made to secure freely given informed consent that participants or their legal representatives have actively provided.

INFORMED CONSENT POLICY
All individuals have individual rights that are not to be infringed. Individual participants in studies have, the right to decide what happens to the (identifiable) personal data gathered, to what they have said during a study, as well as to any photograph that was taken. This is especially true concerning images of vulnerable people (e.g. minors, patients, refugees, etc).
In many instances authors need to secure written consent before including images. Identifying details (names, dates of birth, identity numbers, biometrical characteristics (such as for example facial features) of the participants that were studied should not be published in written descriptions, photographs, and genetic profiles unless the information is essential for scholarly purposes and the participant (or parent/guardian if the participant is a minor or incapable or legal representative) gave written informed consent for publication. Under certain circumstances consent is not required as long as information is anonymized and the submission does not include images that may identify the person.
Informed consent for publication should be obtained if there is any doubt. For example, masking the eye region in photographs of participants is inadequate protection of anonymity.
If identifying characteristics are altered to protect anonymity, such as in genetic profiles, authors should provide assurance that alterations do not
distort meaning.
Exceptions where it is not necessary to obtain consent:
• Images such as x rays, laparoscopic images, ultrasound images, brain scans, pathology slides unless there is a concern about identifying information
in which case, authors should ensure that consent is obtained.
• If images are being reused from prior publications, the Publisher will assume that the prior publication obtained the relevant information regarding
consent. Authors should provide the appropriate attribution for republished images.

DATA SHARING POLICY
Health Problems of Civilization is published in open acces without any requirements or restrictions. Journal is committed to a more open research landscape, facilitating faster and more effective research discovery by enabling reproducibility and verification of data, methodology and reporting standards. We encourage all authors of articles published in our journal to share their research data including, but not limited to: raw data, processed data, algorithms, protocols, methods. All authors willing to share such data have the opportunity to do so and they are made available in the form of supplementary materials.