Slide Format
- Slide Template: You are welcome to use the CROI Content Slide Template (optional) for a professional look that is consistent with the CROI branding.
- Title Slide: A prepopulated title slide is provided for you. See above.
- Format: When preparing your presentation, note that high-definition (HD) projectors will be used for all CROI sessions. Please apply widescreen formatting when preparing your slides (aspect ratio 16:9; resolution 1920 x 1080)
- Font Size: For content slides, it is generally recommended to have a font size of 26 to 32 (based on Arial font) for text. This provides for around 7 lines of text, including a header. Details should be visible from the back of a large ballroom (avoid overly detailed figures or large blocks of text)
- Embedded Videos: Please test any embedded videos in the Speaker Ready room prior presentation.
Use of Trade Names and Promotional Content
Trade names for drugs or products must not be used in presentations. Investigators should refer to drugs, biologics, devices, and other products only by their nonproprietary (generic) names.
Presentations must not include promotional or marketing content. This includes non–science-based promotional language intended to promote or “sell” a product, company, or brand. In addition, presenters may not include QR codes, URLs, or other links that direct attendees to promotional, marketing, or commercial materials.
All content in oral abstract, themed discussion, and poster presentations must remain scientific, objective, and data-focused.
Acknowledgments of Support and Contributors
Acknowledgments of support may be included in the oral presentation of the abstract at CROI.
Sex Stratification and Other Demographic Variables
Presentations from randomized trials and cohorts should follow the ICMJE guidelines, including reporting of study designs (eg, prospective, observational, randomized, double-blind, STROBE, CONSORT, or others), statistical methods, and outcomes by demographic variables. For human clinical or epidemiologic studies, the presentation should provide sex-stratified results or identify who was included if it includes only a single population. Presentations of preclinical data including the use of cell lines and animal studies should include the sex of the animals or the sex of the source of the cell lines. If data are not available on sex (as assigned at birth) or gender (where gender is relevant to the study results), this should be identified as a limitation in the study.
See: ICMJE Preparing for Submission
Use of People-First Language and Appropriate Terminology
See: Appropriate Terminology
Presentations Describing New Compounds
Please be sure to include information sufficient to allow for meaningful review of compound data; this can include isolation, activity, chemical structure, mechanism of action, toxic effects, and pharmacologic data. The chemical or molecular structure must be shown in the presentation (it need not be part of the abstract or be published in the Abstract eBook).