Author Guidelines

For Authors

AMCR Author Guidelines

Prepare the manuscript with the official template for its article type. Initial submissions are assessed by email; manuscripts that pass editorial evaluation are registered in OJS so authors can monitor peer review, revision, and production.

≈47%Indicative acceptance rate
1–3 daysEditorial assessment
3 reviewersDouble-anonymous review
2–4 weeksInitial peer-review cycle

1. Official Manuscript Templates

Choose the official DOCX that matches the manuscript type. Preserve the template's section order, declarations, article-information block, copyright and license statements, and Vancouver reference format.

ORIGINAL RESEARCH

Original Article

For empirical clinical, biomedical, public-health, and related medical research.

Download DOCX
CASE-BASED EVIDENCE

Case Report / Case Study

For a single case, case series, or scientifically framed clinical case study.

Download DOCX
EVIDENCE SYNTHESIS

Systematic Review / Meta-analysis

For PRISMA-aligned systematic reviews, with meta-analysis when appropriate.

Download DOCX

2. Submission Route and Package

Initial submission is by email to editors.amcr@gmail.com.

Send: (1) cover letter; (2) separate title page with complete author names, affiliations, countries, corresponding-author contact and ORCID identifiers where available; (3) anonymized manuscript prepared with the correct AMCR template; (4) editable tables and high-resolution figures; (5) supplementary files; and (6) the applicable reporting checklist. Do not send patient consent forms unless the editor requests them through a confidential channel.

3. General Manuscript Requirements

  • The work must be original, not published previously, and not under consideration elsewhere.
  • Use clear academic English and remove author-identifying information from the anonymized review file.
  • Use a concise sentence-case title. List author names, numbered affiliations, city and country on the separate title page.
  • Provide a structured abstract of no more than 250 words and 3–5 precise keywords. Do not include citations, tables, or figures in the abstract.
  • Arrange the main text as Introduction, Methods, Results, Discussion, Conclusion, Declarations, and References, with article-type-specific subheadings.
  • Number tables and figures in citation order. Provide editable tables, informative captions, defined abbreviations, appropriate units, and high-resolution figures. Remove all patient identifiers.
  • Report numerical results with appropriate precision, confidence intervals, effect estimates, and exact P values when applicable. Do not duplicate every table value in the text.

4. Requirements by Article Type

Original Article

Describe the study design and setting; participants and eligibility; sampling or recruitment; variables, outcomes, measurements, instruments and procedures; quality control; statistical methods, software, missing-data handling and significance threshold; and ethics approval and consent. Results should present participant flow, baseline findings, primary and secondary outcomes, and relevant safety, subgroup, or follow-up findings. Use the reporting guideline appropriate to the design, such as CONSORT, STROBE, STARD, or ARRIVE.

Case Report / Case Study

Follow the CARE guideline or another appropriate case-reporting standard. State the case design, clinical setting and relevant dates; case selection; de-identified patient information; clinical assessment, diagnostic reasoning and differential diagnosis; intervention or exposure; timeline, follow-up, outcomes and adverse events; ethics requirements; and written informed consent for publication. Distinguish observed facts from interpretation and avoid population-level claims unsupported by the case data.

Systematic Review / Meta-analysis

Follow PRISMA 2020. Report the protocol and registration (for example PROSPERO), amendments and review dates; eligibility criteria; databases, registries and other sources with the final search date; a reproducible search strategy; deduplication; independent screening and extraction; risk-of-bias tools; certainty assessment such as GRADE; effect measures; synthesis model and software; heterogeneity; missing-data methods; subgroup and sensitivity analyses; and reporting-bias assessment. Include a PRISMA flow diagram and ensure all counts and pooled estimates are consistent.

5. Ethics, Reporting, and Required Declarations

Research involving humans or animals must identify the approving body, approval or exemption number, consent process, and relevant ethical standard. Clinical trials must provide registration details when required. Use the appropriate reporting checklist and submit it with the manuscript.

Complete every declaration, using an academically appropriate “not applicable” or “none declared” statement where necessary:

  • Statement on the use of artificial intelligence, including tool, version, purpose, verification, and author responsibility when used;
  • Author contributions using author initials and relevant CRediT roles;
  • Funding source, grant number, and sponsor role;
  • Conflict of interest / competing interests;
  • Data availability and repository link or justified restriction;
  • Ethical approval and consent to participate;
  • Consent for publication, especially for identifiable case material;
  • Acknowledgements; and
  • Author approval confirming that all authors approved the final manuscript and accept accountability.

6. References

Use Vancouver style and number references in order of first citation. Write family name followed by initials without periods. For four or more authors, list the first three followed by et al.; list all authors when there are three or fewer. Use Index Medicus journal abbreviations and format DOI as “doi: 10.xxxx”. Verify every citation, DOI, URL, and retraction status. Use at least 15 references when scientifically justified, prioritize primary sources, and favor current literature from the most recent 10 years.

7. Editorial and Publication Workflow

The indicative acceptance rate is approximately 47%. This descriptive rate may change over time and does not predict the outcome of an individual submission. Every decision is based on editorial relevance, originality, methodological quality, ethics, and independent peer review.

01 · Email submission
Authors send the complete submission package to editors.amcr@gmail.com.
02 · Editorial assessment · 1–3 days
The editorial office assesses fit with the Aims and Scope, originality, submission completeness, and similarity. Similarity screening is supported by ORCA; editorial judgment remains with AMCR.
03 · OJS registration
For manuscripts that pass editorial assessment, the journal creates or activates the author's OJS account, registers the submission, and sends account information so progress can be monitored in OJS.
04 · Independent peer review · approximately 2–4 weeks
Three independent reviewers assess the manuscript through a double-anonymous process, focusing on scientific substance, methodological quality, ethics, reporting, and relevance.
05 · Editorial synthesis and decision
The editor evaluates all three reports and decides: accept, minor revision, major revision, or decline.
06 · Author revision · approximately 1–2 weeks
When revision is required, authors submit a revised manuscript and a complete point-by-point response within the stated period.
07 · Reassessment and Letter of Acceptance
Reviewers and the editor reassess the revision. When the scientific and editorial requirements are fully satisfied, AMCR issues the Letter of Acceptance.
08 · Copyediting and proofreading · approximately 1 week
The accepted manuscript enters copyediting and proofreading, supported by EIGO. The edited manuscript is returned to the author for approval.
09 · Galley proof
The journal prepares the galley proof. The corresponding author performs the final check and reports only essential corrections that do not change the accepted scientific content.
10 · Production and publication
After final author approval and production quality control, the manuscript proceeds to publication with complete metadata, DOI, license, and article files.

Ready to submit?

Use the correct template, complete every declaration, and email the full submission package to the AMCR editorial office.

Submit by Email