Human Subjects Research Guidelines

Last Updated: 1 April 2025

The Advanced Journal of Biomedicine & Medicine (AJBM) is committed to protecting the rights, dignity, and welfare of human participants in all biomedical and clinical research. All manuscripts must comply with recognized international and institutional ethical frameworks.

1. Ethical Framework

  • Declaration of Helsinki
  • Belmont Report (Respect, Beneficence, Justice)
  • ICH-GCP Guidelines
  • Applicable national and institutional laws

2. Institutional Review

All studies require IRB or Ethics Committee approval before initiation, with approval number and date cited in the manuscript.

3. Informed Consent

Written informed consent is required unless waived by the ethics committee. Electronic or proxy consent must be justified and approved.

4. Vulnerable Populations

Additional protections must be applied for minors, pregnant women, prisoners, and disadvantaged groups.

5. Privacy & Data Protection

Data must be anonymized or pseudonymized, stored securely, and handled under GDPR or equivalent standards.

6. Clinical Trials

All trials must be registered in recognized registries ↗ and reported according to CONSORT guidelines.

7. Publication Requirements

Manuscripts must include IRB approval details, consent description, registration number, funding, and COI statements.