1. Submit an Abstract
The abstract is what readers review first in order to decide whether the paper is relevant to their work and whether the paper deserves further study. The abstract should provide clear and concise statements on the contents of the paper. It should contain information on what the work is about; how the work is different from other previously-published, related work; a brief discussion on the novelty of the work; the methodology that has been followed; and the theory that has been used to complete the work. The abstract is a self-standing document and should not include references, footnotes, figures (or references to them), or tables (or references to them). It should include brief findings, solutions, impacts, and concluding remarks of the work. The abstract should be written in one paragraph and it should be less than 250 words.
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3. Upload Your Manuscript
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- Uploading your Revised Review Ready Manuscript
- To streamline the process for the second round of reviews please include a written response to each of the reviewers' comments explaining what changes have been made or, if a change was not made, justifying why it was not addressed. This "rebuttal" should be attached as additional pages to the end of the revised draft. With these comments the second round of reviews should go quickly.
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5. Institutional Review Boards
SAE International is committed to ethical and compliant research and publications. Each author has the sole responsibility to confirm approval from the applicable Institutional Review Board (IRB) where necessary and required. All submissions to SAE publications should receive IRB approval in the following cases, including, but not limited to:
- Research involving human subjects: in order to assure the protection of the rights and welfare of human subjects and to ensure the institution and researchers/investigators have complied with applicable regulations
- Any information or product that is subject to FDA approval, testing, or regulation
- Any information or product that is required to follow Department of Health and Human Services (specifically Office for Human Research Protections) guidelines and regulations
- Any information that is part of an application for a product, research, or marketing permit subject to FDA inspection or regulation
IRBs may grant exceptions to these requirements, which the author is required to provide upon request by the Publisher.