Submission of a manuscript to Endoscopy implies that it represents original research not previously published and that it is not being considered for publication elsewhere (see Guidelines for Authors). The corresponding author declares that the manuscript is submitted on behalf of all authors.
If your manuscript submitted to Endoscopy successfully passes the peer review, and is accepted by the editors of the journal, Thieme publishers acquire for the duration of the legal period of protection the exclusive right for the use of the rights of exploitation according to copyright laws, especially also the rights of translation, of publication in special issues, the use of individual passages of text for use in schools, the use for electronic text and visual image communication (also on-line, Internet), use in radio or television programmes, production of microcopies, renting or leasing for a fee or payment, duplication by photomechanical or similar means, storage in electronic databases as well as any other virtual storage and retrieval therefrom, in addition to any processing that may be necessary for the exploitation of the above-mentioned rights. Insofar as the above-mentioned rights are managed by an exploitation company the publisher is entitled to enter into the necessary contracts with the relevant exploitation companies; the publisher is also empowered to enter into contracts with third parties for the exploitation of these rights
With the submission of the manuscript to Endoscopy you as the author confirm that all research involving intervention in human subjects or animals has received the approval of the institutional ethics commitee. If the institution has no formal ethics commitee, you confirm that the terms of the latest version of the Declaration of Helsinki for Medical Research involving Human Subjects have been adhered, and that experiments involving animals adhered to ethical standards.
Product liability laws place a heavy responsibility on you as the author of a scientific publication. This is especially the case when you report on therapeutic modalities and/or drug doses. Thus, please check these details in your manuscript very carefully. Depending on the degree of the theoretically possible dangers, please ask an experienced colleague or co-worker to also check on these details. During the editorial processing of your manuscript by the publisher it will be proof-read several times and, for example, details of doses carefully checked; however, only you as the author have the necessary specialist knowledge to assess the appropriateness of these details. The responsibility for their correctness lies exclusively with you as the author. Together with our authors we want to reduce the risk of possible injury to patients as well of damage claims and liability proceedings. For this we depend on your cooperation.
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