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The Global Journal of Medical and Pharmaceutical Sciences (GJMPS) requires that all research involving human participants, human data, or animal subjects be conducted in accordance with recognized ethical standards and approved by an appropriate ethics committee or institutional review board.
Manuscripts reporting studies involving human participants must include a clear statement confirming that the study received approval from a recognized Institutional Ethics Committee (IEC) or Institutional Review Board (IRB).
The manuscript should provide the following information:
Name of the approving ethics committee or institutional review board
Approval or reference number (if available)
Confirmation that the study was conducted in accordance with ethical guidelines
Authors must also confirm that the study complied with internationally accepted ethical principles for medical research involving human subjects.
Authors must confirm that informed consent was obtained from all participants prior to their inclusion in the study. In the case of minors or individuals unable to provide consent, permission must be obtained from a parent, guardian, or legally authorized representative.
If patient photographs, clinical images, or identifiable information are included in the manuscript, authors must obtain written consent for publication.
Studies involving animals must comply with institutional and national guidelines for the care and use of laboratory animals.
Authors must provide a statement confirming approval from the relevant animal ethics committee and that all procedures were conducted in accordance with accepted animal welfare standards.
Authors are responsible for ensuring that their research complies with ethical standards recommended by organizations such as COPE and ICMJE.
Manuscripts lacking appropriate ethical approval or informed consent documentation may be rejected during editorial review.
All applicable manuscripts must include an Ethics Approval Statement within the methods section confirming ethical approval and consent procedures.