Submissions

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Author Guidelines

Overview

IJMCR publishes peer-reviewed research on medicine, clinical research, diagnostics, translational medicine, public health, and digital health.

Manuscript Requirements

  • Manuscripts must be written in English.
  • Provide a 50 to 150 word abstract and 4 to 6 keywords.
  • Use the journal manuscript template and keep the paper within a recommended maximum of 10 double-column pages.
  • Describe study design, participants, clinical methods, diagnostics, statistical analysis, and approvals clearly.
  • Submit the manuscript in Word, RTF, or PDF. The editorial office may request an editable source file after acceptance.

Submission and Review Flow

  1. Prepare the manuscript using the IJMCR template.
  2. Ensure the file is anonymized if the selected section requires blind review.
  3. Submit through the journal submission workflow in OJS.
  4. Editorial screening checks scope, formatting, originality, and completeness.
  5. Eligible manuscripts are reviewed by at least two independent reviewers.
  6. Revisions, the signed copyright form, and publication fee processing are completed only after acceptance.

Required Downloads

Journal-Specific Expectations

  • Include ethics approval, informed consent, and trial registration details where applicable.
  • Describe participant selection, interventions, diagnostics, and statistical methods clearly.
  • Report limitations, clinical relevance, and patient-safety considerations honestly.

Publication Fee

USD 100 is charged only for accepted papers. No submission fee is charged.

Submission Preparation Checklist

All submissions must meet the following requirements.

  • The manuscript is original, has not been published previously, and is not under review elsewhere.
  • The submission file is in Word, RTF, or PDF format and follows the journal template referenced in the Author Guidelines.
  • The manuscript includes title, abstract, keywords, main text, references, and any required statements on funding, conflicts of interest, and data availability.
  • Study design, participant selection, diagnostics, interventions, and statistical methods are described clearly.
  • Where applicable, ethics approval, informed consent, trial registration, and patient-safety statements are included.
  • The conclusions are consistent with the evidence and clinical limitations are discussed honestly.
  • Blind-review instructions have been followed where required.

Privacy Statement

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