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Reporting Guideline Compliance

Reporting Checklist Review

Pubrica’s reporting checklist review is for authors preparing a manuscript for journal submission. Our reporting guideline specialists check your manuscript item by item against the guideline for your study type and deliver the completed checklist, with page and line references and a list of missing items. Journals request this checklist and reviewers compare it with the paper, so an entry that points to content the manuscript does not contain can undermine confidence in the whole submission.

  • The right guideline for your study type: CONSORT 2025 for trials, PRISMA 2020 for reviews, STROBE for observational studies and a dozen others
  • Item by item against the manuscript, with the page and line reference for every item present
  • Missing items identified with what would satisfy them, so that each gap can be closed with a short addition
  • The current version: CONSORT and SPIRIT were updated to 2025 versions last year, and a checklist based on the 2010 version is out of date
  • The completed checklist delivered, in the form your journal takes
Scope of the Checklist Review Included services and exclusions

Guideline identified for your study typeIncluded

Item-by-item check against the textIncluded

Missing items with remediesIncluded

Completed checklist deliveredIncluded

Writing the missing contentQuoted separately

Study type → guideline → checked → located → checklist

Every review
  • Guideline matched to the study type
  • Checked against the manuscript text
  • Page and line for every item
  • Missing items given a remedy
  • Current versions only
Quoted per manuscriptOn study type and checklist length
By guidelineCONSORT 2025, PRISMA 2020, STROBE and others
Current versionsCONSORT and SPIRIT 2025, not 2010 and 2013
ISO 9001:2015Quality management certified · cert. H3CR9TCU20251212INDQM10N

Deliverables

Four Components of Every Reporting Checklist Review

Each review covers four components. The study design determines which checklist applies.

Guideline identification for your study type A randomised trial, a systematic review, a cohort study, a diagnostic accuracy study, a prediction model and a case report are governed by six different checklists.

Identification exampleSubmitting a PRISMA checklist for a cohort study, or a CONSORT checklist for a non-randomised comparison, indicates to reviewers that the guideline was not applied correctly.

Checked against the text, item by item Each item is confirmed as present with a page and line reference, or recorded as absent. No item is marked as present on assumption.

Review exampleItem 6a: Completely defined pre-specified primary outcome. Page 7.Item 6a: the primary outcome is named on page 7 but not defined — no measurement method, no timepoint. Not satisfied as written. One sentence fixes it.

Missing items with a remedy attached Each gap is accompanied by a description of what would satisfy it, so it can be resolved with a short addition rather than further interpretation of the guideline.

Findings exampleMost missing items require a single sentence. A few indicate information that was not recorded during the study, and these are best identified before a reviewer raises them.

The current version of the guideline CONSORT and SPIRIT were both updated to 2025 versions last year, and PRISMA has used the 2020 version for some time. Many templates in circulation have not been updated.

Version check exampleA checklist based on a superseded version indicates an outdated template, and reviewers notice this.

Samples are illustrative and anonymised. Hover over a sample to replay it.

Compliance and Standards

Reporting Guidelines and Quality Standards by Study Design

The EQUATOR Network catalogues these guidelines. The study type determines which applies, and some studies require more than one.

CONSORT 2025 and SPIRIT 2025 (trials and protocols)

Randomised trial reporting and trial protocols. Both moved to 2025 versions last year, replacing CONSORT 2010 and SPIRIT 2013.

PRISMA 2020

PRISMA 2020 (reviews and meta-analyses)

Systematic review and meta-analysis reporting, including the twelve-item abstract checklist and the flow diagram.

STROBE and others

Observational and other designs (STROBE, STARD, ARRIVE 2.0, CARE, COREQ, SQUIRE 2.0, TRIPOD+AI)

Cohort and case-control studies, diagnostic accuracy, animal research, case reports, qualitative research, quality improvement and prediction models.

ISO9001:2015

Quality management (cert. H3CR9TCU20251212INDQM10N)

Our quality management system governs how work is managed, recorded and released.

Responsible Use of AI

Our Approach to AI Use and Disclosure

Journals now ask authors to declare any AI tools used in preparing a manuscript. Pubrica treats this declaration as part of the deliverable and tells you exactly what was used on your manuscript, so that you can complete it accurately.

How we use AI toolsWe use automated tools for similarity screening, for consistency of terms, figures and cross-references, for checking references against the records they cite, and for reformatting to a journal template.
What we do not use AI forWe do not use AI to write or strengthen your argument or to draft rebuttal reasoning. We also do not provide AI-detection scores, because no tool produces them reliably and false positives disproportionately affect authors writing in English as an additional language.
What your AI declaration includesThe declaration states the tool, the stage at which it was used and the human oversight applied. Journals, funders, regulators and the ICMJE January 2026 update now expect this, and an undeclared tool discovered later is treated as an integrity matter.

Why We Do Not Publish AI Accuracy Figures

Accuracy figures for AI tools are usually reported by the companies that sell them.

Pubrica therefore quotes no self-generated accuracy figure, as it would carry the same conflict of interest. Instead, we tell you which tool was used on your project, at which stage, and what a human editor changed afterwards.

How It Works

How Our Reporting Checklist Review Process Works

The review has three steps: identifying the guideline, checking each item and completing the checklist. The item-by-item check takes the most time and cannot be shortened.

Step one

Identify the guideline

We identify the guideline from the study design rather than from how the authors describe it, and where more than one applies, we check all of them.

Step two

Check item by item

Every item is located in the manuscript with a page and line reference, or recorded as absent with a note of what would satisfy it.

Step three

Complete and deliver

We complete the checklist in the form your journal requires and supply a gap list so that you can address missing items before submission.

Our experts

Our Reporting Checklist Review Team

The same named team works on your project from scoping to delivery, and your project coordinator introduces each member before work begins.

Subject matter expertClinical or scientific expert matched to your topic

Reviews the scientific content for accuracy and confirms that each conclusion is supported by the evidence. The expert is matched to your field.

OwnsScientific accuracy and interpretation
Reads againstThe journal's instructions and reporting guideline
FieldMatched to your topic
Senior editorEdits for language, structure and consistency

Edits for clarity, grammar, structure and consistency while preserving the author voice and scientific meaning.

OwnsLanguage, structure and consistency
Reads againstThe journal style and a project style sheet
OutputTracked-changes manuscript
Second reviewerIndependent quality check before delivery

Checks the finished work independently against the agreed scope and the applicable checklist. Findings are logged and resolved before delivery.

OwnsIndependent quality control
Reads againstThe agreed scope and checklist
Signed off byProject lead
Project coordinatorYour single point of contact

Manages the timeline, keeps you informed at each stage and coordinates the team so that questions are answered and deadlines are met.

OwnsTimeline and communication
Reads againstYour brief and deadline
OutputDelivery and follow-up

Packages

Reporting Checklist Review Packages

The cost depends on the study type and the length of the checklist; for example, a CONSORT review is longer than a CARE review.

Review

Checklist review

Any manuscript with a reporting guideline

Quoted per projectOn study type and checklist length

Delivery By scope

  • ✓Guideline identified from the study design
  • ✓Item-by-item check against the manuscript
  • ✓Page and line for every satisfied item
  • ✓Missing items with remedies
  • ✓Completed checklist in your journal’s form

Where more than one guideline applies, all of them are checked.

Deliverables Request a quote
Review + fix

Review with remediation

Manuscripts with gaps to close before submission

Quoted per projectOn the number and nature of gaps

Delivery By scope

  • ✓Everything in the review
  • ✓Missing items written into the manuscript
  • ✓Structural changes where an item needs one
  • ✓Re-checked after the additions
  • ✓Final checklist delivered

Where an item is missing because something was not recorded during the study, we say so rather than writing around it.

Deliverables Request a quote

Send your manuscript and we will check the first ten checklist items free of charge. This check will also show whether your checklist template still cites CONSORT 2010.

FAQs

Reporting Checklist FAQs

If your question is not answered here, please ask an expert. No quote is required.

The checklist follows from the study design. Randomised trials use CONSORT 2025, systematic reviews PRISMA 2020, observational studies STROBE, diagnostic accuracy studies STARD, animal research ARRIVE 2.0, prediction models TRIPOD+AI, case reports CARE and qualitative research COREQ.

Some studies require more than one, such as a systematic review of diagnostic accuracy studies. We identify all applicable guidelines from the design rather than from the title.

Yes, and many authors do, often from memory. However, it is easy to enter a page number for an item that the manuscript does not actually satisfy.

A reviewer who follows one reference and finds nothing is likely to check all of them, and an inaccurate checklist then weakens the submission.

In that case we state that it cannot be satisfied and explain why. Some items do not apply to a given design, and marking them as not applicable with a reason is acceptable.

Occasionally an item is missing because information was not recorded during the study. This cannot be addressed by rewording, and you should be aware of it before a reviewer raises it.

It may be. CONSORT and SPIRIT were both updated to 2025 versions last year, and many templates in circulation have not been updated.

A checklist based on CONSORT 2010 indicates an outdated template, which is easily avoided.

Request a Free Check of the First Ten Checklist Items

This check will also show whether your checklist template still cites CONSORT 2010.

Get a free quote

Regulations

Check your project against this rule

  1. 1Your work
  2. 2Your details
  3. 3Send
What do you need?

Material you send is held under signed confidentiality, with access limited to the assigned team and encrypted transfer. It is not used to train anything and is not passed to third-party tools. Ask for the agreement before you send anything you would rather cover first.