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Journal Guides12 min readUpdated Jun 7, 2026

Diagnostics Submission Guide: MDPI Process (2026)

A package-readiness guide to submitting to Diagnostics (MDPI): section-scope fit, the SuSy portal, the editorial pre-check, single-blind review, STARD/TRIPOD reporting, and the CHF 2,600 APC.

Author contextAssociate Professor, Clinical Medicine & Public Health. Experience with NEJM, JAMA, BMJ.View profile

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How to approach Diagnostics

Use the submission guide like a working checklist. The goal is to make fit, package completeness, and cover-letter framing obvious before you open the portal.

Stage
What to check
1. Scope
Confirm a clear diagnostic angle and the right Section
2. Package
Map reporting onto STARD, TRIPOD, PRISMA, or CARE
3. Cover letter
Report accuracy metrics with confidence intervals and a reference standard
4. Final check
Submit through the MDPI SuSy portal with ethics and data statements

Quick answer: This Diagnostics submission guide starts with the upload reality: submit through the MDPI SuSy portal, where every manuscript first hits an editorial pre-check for section-scope, ethics, and soundness before single-blind review. Diagnostics has a 2024 impact factor of 3.3, charges a CHF 2,600 APC, and returns a first decision in roughly 22 days.

The journal runs a fast, soundness-based model, not a selectivity filter, so the package that clears pre-check has a clear diagnostic angle, a matching reporting checklist (STARD, TRIPOD, PRISMA, CARE), complete ethics and data statements, and accuracy metrics with confidence intervals.

When is Diagnostics a realistic target?

This Diagnostics submission guide covers what actually decides the outcome. If you are preparing a Diagnostics submission, the main risk is rarely whether the science is impressive enough. The main risk is whether the manuscript clears the editorial pre-check: a fast, template-driven screen for section fit, ethics completeness, and reporting integrity that happens before any reviewer reads the paper.

Diagnostics is a realistic target when four things are already true:

  • the central question is genuinely about diagnosis, prognosis, or a diagnostic test, not a basic-science study with a diagnostic label added late
  • the study maps cleanly onto a section (Medical Imaging, Clinical Laboratory Medicine, Pathology and Molecular Diagnostics, Clinical Diagnosis and Prognosis, Point-of-Care Diagnostics, Diagnostic Microbiology, or Machine Learning and Artificial Intelligence in Diagnostics)
  • the ethics, institutional review board, informed-consent, and data availability statements are complete and specific
  • the reporting follows the guideline that matches the design (STARD for accuracy studies, TRIPOD or TRIPOD-AI for prediction models, PRISMA for reviews, CARE for case reports)

If one of those is missing, the speed that makes Diagnostics attractive works against you: the pre-check filters incomplete packages quickly.

Before you spend the submission, use the Diagnostics manuscript fit check to test whether the section angle, declarations block, and reporting compliance will clear MDPI's pre-check.

Evidence boundary: across N=12 Manusights first-party evidence review units for this Diagnostics page, the recurring fit issue was whether the title, abstract, section choice, reference standard, validation plan, checklist, ethics block, and cover letter prove a diagnostic claim rather than a general clinical or biology finding. Production Manusights preview data does not yet provide a large enough Diagnostics-specific cohort to quote an anonymized outcome rate, so this guide uses official MDPI guidance plus first-party submission-fit analysis.

What should a Diagnostics submission package show before upload?

What to pressure-test
What should already be true before upload
Section-scope fit
The manuscript reads as a diagnostic or prognostic study and maps to one named Diagnostics section, not a basic-science paper relabeled.
Reporting checklist
The design-appropriate guideline (STARD, TRIPOD, TRIPOD-AI, PRISMA, CARE) is followed and the completed checklist is supplied.
Accuracy metrics
Sensitivity, specificity, and AUC are reported with confidence intervals, against a clearly defined reference standard.
Validation strategy
A diagnostic-AI or prediction model has external or temporal-geographic validation, not internal cross-validation alone.
Ethics package
Institutional review board approval, informed consent, and animal-ethics statements are complete and specific.
Data availability
A data availability statement names a repository, accession, or a concrete access route, not "available on request" alone.
Declarations block
Author Contributions, Funding, and Conflicts of Interest statements are drafted before upload, not after acceptance.

Source: Diagnostics Instructions for Authors and MDPI research and publication ethics policy (accessed June 2026)

What makes Diagnostics a distinct target?

Diagnostics is not a stronger version of a subscription radiology or laboratory-medicine journal, and it is not a weaker one. It is a different model. MDPI built it around speed and soundness-based review: the editorial question is whether the work is methodologically sound, in scope, and correctly reported, not whether it ranks among the most selective diagnostic findings of the year. That model shapes everything about how you should prepare the package.

It helps to anchor the soundness-versus-selectivity distinction against journals authors already know. At a flagship clinical title like The Lancet, JAMA, or NEJM, the editorial question is whether the result should change practice, and most submissions are desk-rejected for novelty before reporting is ever assessed; the bar at Nature-tier journals is similar but for biological reach. Diagnostics inverts the order.

A correct, complete, in-scope diagnostic study clears the bar even when the finding is incremental, so the leverage is not in pitching importance the way you would for The Lancet or JAMA. It is in proving the diagnostic claim is reported and validated to the standard the field expects.

Three consequences matter most.

  • Diagnostics is strongly section-based, so scope fit is assessed against a named diagnostic discipline rather than a vague "is this interesting" bar.
  • The pre-check is fast and partly template-driven, so completeness is rewarded and incompleteness is punished early.
  • Reporting guidelines are load-bearing: a paper that claims diagnostic accuracy but does not report it the STARD way reads as not ready, even when the underlying data are good.

A technically interesting model with a missing STARD checklist, or a single-center retrospective study claiming clinical deployability with no external validation, can be returned or sent straight to major revision before it gains any momentum. A competent, complete, in-scope study with metrics reported correctly moves quickly.

The core fit for most submissions is the original research article. It works best when the diagnostic or prognostic question is central, the reference standard is explicit, the methods are reproducible from the text, and the declarations and reporting package are complete on first upload.

Ask these questions before you submit:

  • is a diagnostic or prognostic question the actual subject of the paper, or is diagnosis a downstream application of a basic-science finding?
  • can a reader reproduce the analysis from the manuscript and supplementary files alone, including the reference standard?
  • are the accuracy metrics reported with confidence intervals, or as bare point estimates?
  • does the reporting follow the checklist that matches the study design?

If the answers are uncertain, the pre-check problem is usually more important than the science problem.

What are Diagnostics editors actually screening for?

The pre-check editor is answering a short list of questions fast.

On scope, the editor asks whether the manuscript belongs in a diagnostics journal and in which section. If the diagnostic relevance is thin or bolted on, the paper is redirected or returned. On soundness, the question is whether the design supports the diagnostic claim: is there a reference standard, is the spectrum of patients representative, are the metrics appropriate for the question. Diagnostics does not require the finding to be field-defining, but it does require the work to be done and reported correctly.

On integrity, the editor checks whether ethics approvals, consent, image-integrity expectations, and data availability are in order. MDPI runs integrity and plagiarism checks at pre-check, and gaps here trigger fast returns. On completeness, the editor looks for the declarations block and the design-appropriate reporting checklist. A diagnostic-accuracy study with no STARD checklist, or a prediction model with no TRIPOD statement, reads as not ready, even when the science is fine.

How should you build the submission package around the editorial decision?

Manuscript structure: Diagnostics expects a defined section set: Abstract, Keywords, Introduction, Materials and Methods, Results, Discussion, Conclusions, plus the declarations block. Original research and systematic reviews need a structured abstract of around 200 to 250 words. The abstract is the first thing the pre-check editor reads, so the diagnostic question, the reference standard, and the headline accuracy result (with its confidence interval) all need to be visible there.

Reporting and methods readiness: Provide full methodological detail so results can be reproduced, and follow the design-appropriate guideline. STARD governs diagnostic-accuracy studies; TRIPOD (and TRIPOD-AI for machine-learning models) governs prediction-model development and validation; PRISMA governs systematic reviews and meta-analyses (with a registered protocol); CARE governs case reports. A diagnostic or prediction-model paper that does not map cleanly onto its reporting checklist is the most common reviewer-stage friction point.

Declarations and ethics: Draft the Institutional Review Board statement, Informed Consent statement, Author Contributions (by initials), Funding, Data Availability, and Conflicts of Interest sections before you upload. These are not post-acceptance paperwork at MDPI; they are pre-check gates. For retrospective imaging or laboratory studies, the consent or consent-waiver language has to be explicit.

Figures, supplementary, and abstract assets: A graphical abstract is optional but commonly used; if supplied, it should be a high-resolution PNG, JPEG, or TIFF. Supplementary materials should carry the completed reporting checklist, the full confusion matrix or calibration data, and detail that would slow the main narrative. ORCID is expected for the submitting author, and the system will ask for suggested reviewers in the relevant diagnostic subspecialty.

Common failure patterns at Diagnostics

In our pre-submission review work with Diagnostics manuscripts, four failure patterns generate the most consistent pre-check returns and reviewer friction, and each one is testable against your own manuscript before you upload. Across the diagnostics and imaging manuscripts we pre-screen, the single most common reason a technically sound paper draws a major-revision verdict is a model or accuracy claim that the validation evidence does not support, not a flaw in the underlying science.

Across our diagnostics and clinical pre-submission reviews, the pattern that surprises authors most is that the Diagnostics pre-check is not a selectivity filter in the Clinical Chemistry sense; it is a fit-and-completeness filter where the reporting guideline does most of the work. The manuscripts that get returned fastest are rarely bad science. They are competent studies whose section angle, declarations block, accuracy reporting, or validation strategy is not ready for a fast, template-driven screen. Manuscripts coming through pre-submission review for Diagnostics split along these four lines.

Scope-thin diagnostic framing that the section editor cannot place

The single most common pattern we see is a manuscript whose diagnostic relevance is downstream rather than central. The study is really a cell-biology, bioinformatics, or methods paper, and a diagnostic angle (a biomarker panel, a classifier, a TCGA-style dataset) has been added so the work can target a diagnostics journal.

Diagnostics is strongly section-based, so the pre-check editor has to place the manuscript in a specific section. When the diagnostic question is not the actual subject, the section assignment fails and the paper is returned or redirected fast.

The testable version: read your own abstract and introduction, and ask whether a section editor could name the Diagnostics section from the first paragraph alone. If the diagnostic application only appears in the discussion, rebuild the introduction and abstract around the diagnostic question and the reference standard rather than around the underlying biology or method.

Check whether your Diagnostics scope angle reads as diagnostic from the abstract →

A diagnostic-AI model with no external validation, framed as clinically deployable

The second pattern is specific to this journal because so much of its volume is machine learning and imaging. We repeatedly see a model trained and tested on a single-center retrospective dataset, evaluated only with internal cross-validation, and then framed in the discussion as ready for clinical deployment.

Reviewers in this space now expect external or temporal-geographic validation. Its absence is the common reason a methodologically clean model gets major revision instead of acceptance.

The testable version: if your paper claims clinical utility, confirm the model was validated on data it never saw during training and tuning, ideally from a different site, scanner, or assay. If the only evidence is internal cross-validation on one cohort, frame the manuscript as a development study and map it against STARD-AI or TRIPOD-AI before submission.

Check whether your Diagnostics model claims match its validation evidence →

Accuracy metrics reported as bare point estimates without a reference standard

The third pattern is diagnostic-accuracy reporting that does not meet the bar STARD sets. We see sensitivity and specificity reported as single numbers with no confidence intervals, AUC values quoted without a comparison or a defined positive class, and no clear definition of the reference standard against which accuracy is measured.

In diagnostics, the reference standard is the whole argument: an AUC of 0.95 means nothing if the ground truth is itself uncertain or circular.

The testable version: for every accuracy number in your abstract and results, confirm there is a confidence interval, the reference standard is named and justified, and the patient spectrum is described well enough for a reader to judge generalizability.

Check whether your Diagnostics accuracy metrics meet the STARD bar →

Reporting that does not map onto its guideline checklist

The fourth pattern shows up at the reviewer stage: reporting that does not follow the checklist matching the study design. Examples include a diagnostic-accuracy study with no STARD flow diagram, a prediction model with no TRIPOD statement, a systematic review with no PRISMA diagram and no registered protocol, or a case report that ignores CARE.

Each one forces reviewers to spend their attention on missing structure rather than on the science. In diagnostics, clinical relevance depends on how the reference standard, sample size, and statistical analyses are reported.

The testable version: identify the guideline that matches your design, walk your manuscript against every checklist item, and supply the completed checklist and relevant diagram in the supplementary files. If half your checklist items point to "see Methods" without the Methods actually covering them, the reporting is not ready.

Check whether your Diagnostics reporting matches its guideline checklist →

Each of these is something you can check against your own draft before you commit the submission. This guide tells you what Diagnostics editors look for; the review tells you whether YOUR paper passes the pre-check before you upload.

Of 60+ manuscripts our team reviewed for diagnostics, laboratory-medicine, and imaging journals, including Diagnostics and its open-access peers, the recurring pre-check weakness was a diagnostic claim whose section fit, validation evidence, or reporting checklist did not match the abstract. Paid Manusights reviews include a 60-day money-back guarantee, and we do not train models on submitted manuscripts. Run a [Diagnostics submission package check](/ai-review?

target_journal=Diagnostics&source_blog=diagnostics-submission-guide&primary_concern=submission_readiness) to see whether your scope framing, validation strategy, accuracy reporting, and declarations block will clear the MDPI pre-check.

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What is the editorial triage timeline at Diagnostics?

Diagnostics reports a median first decision near 22 days and median acceptance-to-publication near 2.7 days. Treat these as planning ranges, not promises: clinical imaging and large diagnostic-accuracy manuscripts often run longer because finding reviewers with the right subspecialty takes time.

  • Day 0: Submission via SuSy. The portal accepts the package and routes it to the section editor for pre-check.
  • Days 1 to 3: Editorial pre-check. The editor screens section-scope fit, ethics completeness, integrity and plagiarism checks, reporting-checklist presence, and basic soundness.

The fastest returns happen here, before any reviewer is invited.

  • Days 3 to 7: Reviewer invitation. Manuscripts that pass pre-check enter single-blind reviewer search, typically targeting two or more reviewers in the relevant diagnostic subspecialty.
  • Days 7 to 22: Peer review and first decision. Reviewer reports return and the editor issues the first decision, with a median near 22 days from submission.

Major revision is the most common outcome for papers that clear pre-check.

  • Days 22 to 40: Revision and acceptance. Revisions are usually requested on a short clock; resubmission and a second review cycle commonly land acceptance inside a few weeks for in-scope, complete packages.
  • Days 40 to 43: Production and publication. Acceptance to publication runs near 2.7 days at median, so the slow part of the calendar is reviewer search and revision, not production.

What does the Diagnostics submission portal require?

Once the science and framing are ready, here is what the SuSy portal actually expects.

Manuscript file: Submit through the MDPI SuSy submission system using the Diagnostics Microsoft Word template or LaTeX. The structured abstract for original research and systematic reviews runs to around 200 to 250 words, with 3 to 10 keywords. State the diagnostic question, the reference standard, and the headline accuracy result with its confidence interval in the abstract.

Required statements: Every submission needs Author Contributions (by author initials), a Funding statement, an Institutional Review Board statement, an Informed Consent statement where human subjects are involved, a Data Availability Statement, and a Conflicts of Interest disclosure. These appear as a structured declarations block at the end of the manuscript.

Reporting checklists: Supply the design-appropriate completed checklist and diagram (STARD for diagnostic accuracy, TRIPOD or TRIPOD-AI for prediction and machine-learning models, PRISMA with a registered protocol for systematic reviews, CARE for case reports) as supplementary files.

Suggested reviewers and ORCID: The system asks for suggested reviewers in the relevant diagnostic subspecialty and expects an ORCID for the submitting author. Co-author ORCIDs are encouraged.

Graphical abstract and supplementary: A graphical abstract is optional; if supplied, use a high-resolution PNG, JPEG, or TIFF at a minimum of 560 by 1100 pixels. Figures should be supplied at high resolution, and large imaging datasets or model artifacts should be split into clearly named supplementary files rather than bundled into one hard-to-review upload. There is no fixed cap on the number of figures, but a research article with more than 8 figures usually signals that the main diagnostic story is not yet focused.

What is the Diagnostics pre-submission checklist?

  • [ ] The abstract and introduction make the diagnostic question central, with the Diagnostics section clear from the first paragraph
  • [ ] The reference standard is named and justified, and accuracy metrics (sensitivity, specificity, AUC) carry confidence intervals
  • [ ] Any prediction or machine-learning model has external or temporal-geographic validation, not internal cross-validation alone
  • [ ] The Institutional Review Board, Informed Consent, and animal-ethics statements carry real approval identifiers
  • [ ] The Data Availability Statement names a repository, accession, or concrete access route
  • [ ] The design-appropriate reporting checklist (STARD, TRIPOD, TRIPOD-AI, PRISMA, CARE) is followed and supplied
  • [ ] The full declarations block (Author Contributions, Funding, Conflicts of Interest) is drafted before upload
  • ] Run a [Diagnostics submission readiness check to confirm the package will clear MDPI's pre-check

How does Diagnostics compare with peer diagnostics journals?

Diagnostics competes with other diagnostics and laboratory-medicine venues on speed, breadth, and open access rather than selectivity. The comparison that matters is review model, cost, scope, and selectivity, not the raw citation metric.

Journal
2024 IF
APC
Review model and scope angle
Diagnostics (MDPI)
3.3
CHF 2,600
Single-blind, fast soundness-based; broad diagnostics, section-based across imaging, lab, pathology, AI
Journal of Clinical Medicine (MDPI)
2.9
CHF 2,600
Single-blind, soundness-based; broad clinical medicine, less diagnostics-specific
Clinical Chemistry (AACC)
9.3
~$3,500 (OA option)
Single-blind, highly selective; laboratory medicine and biomarker validation
European Radiology (ESR)
4.7
~$3,290 (hybrid OA)
Single-blind, selective; imaging research and technical innovation

Source: Clarivate JCR 2024 and each journal's published author and fee pages (accessed June 2026)

Diagnostics vs Journal of Clinical Medicine: Both are broad MDPI open-access medical titles with similar economics and speed. The editorial difference is focus: JCM wants clinical-medicine work across specialties, while Diagnostics wants the diagnostic or prognostic test to be the protagonist. If your study is fundamentally about how well a test, image-analysis pipeline, or biomarker discriminates disease, Diagnostics is the better section fit; if it is a broader clinical-outcomes study where diagnosis is incidental, JCM routes more cleanly.

Diagnostics vs Clinical Chemistry: These are not the same kind of venue. Clinical Chemistry is a highly selective AACC flagship that wants rigorously validated laboratory-medicine and biomarker work, often with analytical validation and multi-cohort evidence; it rejects far more than it accepts and turns around slower. Diagnostics is faster and far more accepting at the soundness bar.

If your biomarker study is a strong but single-cohort development effort, Diagnostics is realistic and Clinical Chemistry usually is not; if you have multi-site analytical and clinical validation, Clinical Chemistry is the higher-prestige target worth the longer odds.

Diagnostics vs European Radiology: European Radiology is the selective ESR flagship for imaging, and it expects imaging research with clinical depth and methodological rigor, frequently multi-reader or multi-center. Diagnostics' Medical Imaging and Theranostics and Machine Learning sections accept imaging and radiomics work on a soundness basis at lower selectivity. If your imaging-AI study is a single-center development paper, Diagnostics is the realistic home; if it is a multi-center reader study with external validation, European Radiology is the stronger-brand target.

Submit If

  • a diagnostic or prognostic question is genuinely central to the study, and a section editor could name the Diagnostics section from the title and abstract
  • the reference standard is explicit and the accuracy metrics carry confidence intervals
  • any model has external or temporal-geographic validation, and the claims match the validation evidence
  • the ethics, consent, and data-availability statements are complete before upload, and a fast, soundness-based decision with full open access fits your timeline and budget

Think Twice If

  • the diagnostic angle only appears in the discussion or as a future application, and a section editor could not name the subfield from the title and abstract
  • you are claiming clinical deployability for a model validated only with internal cross-validation on a single-center retrospective dataset, with no external test set
  • the accuracy metrics are bare point estimates with no confidence intervals, against a reference standard that is undefined or circular
  • the declarations block and data availability statement are still empty stubs, with no IRB number, no consent language, and no named repository
  • you need a highly selective venue for a fully validated, multi-cohort diagnostic, in which case Clinical Chemistry or European Radiology is the better target

How was this Diagnostics guide built?

This guide was researched and built from primary sources: the sources we checked include the Diagnostics Instructions for Authors, the journal's aims-and-scope, sections, and editorial-process pages, MDPI's research and publication ethics policy, the STARD and TRIPOD reporting-guideline statements, and Manusights pre-submission review patterns from diagnostics and imaging manuscripts deciding between Diagnostics and peer open-access and selective diagnostics journals. We reviewed and compared current MDPI author guidance with recent Manusights work reviews from authors weighing Diagnostics, Journal of Clinical Medicine, Clinical Chemistry, and European Radiology. Last reviewed by the Manusights clinical editorial team on 2026-06-07.

Source limitations: MDPI can update the APC, article-format details, abstract caps, and editorial-process numbers after this review date, so verify final administrative details against the official Diagnostics author pages before upload. Median timelines are reported by the journal and vary by subspecialty. Use this guide for the decision the official instructions cannot answer: whether your scope framing, validation strategy, accuracy reporting, and declarations block are ready for the MDPI pre-check.

Before you upload, run your manuscript through a Diagnostics submission readiness check to catch the scope, validation, accuracy-reporting, and ethics gaps the MDPI pre-check filters for. The check is free to run (/ai-review) and takes a single upload.

Frequently asked questions

Diagnostics reports a median time to first decision of roughly 22 days from submission, with median acceptance-to-publication near 2.7 days. That speed is the journal's defining feature: it runs a fast, soundness-based single-blind review rather than a slow selectivity filter.

Diagnostics is a fully gold open-access journal. An article processing charge of CHF 2,600 applies to manuscripts accepted after peer review. There is no subscription route and no submission fee. Discounts are available through MDPI's Institutional Open Access Program (IOAP) and for members of affiliated societies, so check whether your institution has an IOAP agreement before you budget the full APC, and verify the current figure on the journal's APC page because MDPI updates it periodically.

Diagnostics publishes original research articles, reviews, systematic reviews and meta-analyses (PRISMA), communications, case reports (CARE), interesting images, protocols, and several other formats. Original research and reviews are the core. Pick the type that matches your evidence: a single validated diagnostic finding fits a communication, a diagnostic-accuracy study belongs in an original article reported against STARD, a prediction or machine-learning model maps onto TRIPOD or TRIPOD-AI, and a comprehensive synthesis belongs in a systematic review with a registered protocol.

Diagnostics uses single-blind peer review: reviewers see author identities, but reviewer identities are not disclosed to authors. Every submission first passes an editorial pre-check for section-scope fit, ethics, integrity, and basic soundness before it reaches reviewers. The pre-check is where most fast rejections happen, so section fit, complete ethics statements, and a reporting checklist that matches the study design all matter before the manuscript ever reaches an external reviewer.

The most common pre-check rejections are section-scope mismatches where the diagnostic angle is thin, missing or incomplete ethics and institutional review board statements, absent data availability statements, and diagnostic or prediction-model work that does not follow the relevant guideline (STARD, TRIPOD, TRIPOD-AI, PRISMA, CARE). A diagnostic-AI model with no external validation, or a single-center retrospective accuracy claim framed as clinically deployable, is also commonly returned or sent back for major revision, because the reporting and the evidence do not match the claim.

References

Sources

  1. Diagnostics Instructions for Authors
  2. Diagnostics journal home and editorial process
  3. Diagnostics Aims and Scope
  4. Diagnostics Article Processing Charges
  5. Diagnostics journal sections
  6. MDPI SuSy submission system
  7. STARD-AI reporting guideline (Nature Medicine)

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