Policies
Journal Policies – Frontiers in Pharmacological Research (FPR)
1. Open Access Policy
Frontiers in Pharmacological Research (FPR) follows a fully open-access publishing model. All articles are freely available online immediately upon publication without any subscription or access fees.
Readers are permitted to read, download, copy, distribute, print, search, or link to the full texts of articles without prior permission, provided proper citation is given.
2. Plagiarism Policy
FPR maintains a strict zero-tolerance policy towards plagiarism.
- All submissions are checked using plagiarism detection tools such as Turnitin/iThenticate
- Manuscripts with significant plagiarism will be rejected immediately
- If plagiarism is detected post-publication, the article will be retracted
Authors must ensure originality and proper citation of all sources.
3. COPE Guidelines for Plagiarism
The journal follows Committee on Publication Ethics (COPE) guidelines.
Actions may include:
- Minor plagiarism → revision request
- Moderate → rejection
- Severe → retraction + author blacklist
4. Copyright Policy
Authors retain copyright of their work.
However, authors grant FPR:
- Right to publish and distribute the article
- Right to archive and index the work
Authors can reuse their work with proper citation.
5. Rights and Grants to Authors
Authors are allowed to:
- Share published articles on personal/institutional websites
- Use content for teaching, presentations, and future research
- Deposit in repositories
6. Licensing Policy
All articles are published under:
Creative Commons Attribution License (CC BY 4.0)
This allows:
- Sharing
- Adaptation
- Commercial use
With proper attribution.
7. COPE Conflict of Interest Policy
All participants must disclose conflicts:
- Authors → funding, affiliations
- Reviewers → competing interests
- Editors → unbiased decisions
Failure to disclose may lead to rejection or retraction.
8. Publication Ethics & Malpractice Statement
FPR follows strict ethical standards:
- No fabrication or falsification
- No duplicate submissions
- Confidential peer review
- Transparent editorial decisions
Misconduct is handled per COPE standards.
9. APC (Article Processing Charges) & Waiver Policy
FPR may charge APC for publication.
Waivers are available for:
- Students
- Researchers from low-income regions
- Exceptional cases
Requests are reviewed by the editorial board.
10. Withdrawal Policy
- Before review → free withdrawal
- During review → valid reason required
- After acceptance → not allowed (except serious issues)
Published articles can only be retracted, not withdrawn.
11. Human and Animal Rights Policy
For applicable research (especially in pharmacology, toxicology, and experimental drug studies):
- Must follow ethical standards (e.g., Declaration of Helsinki)
- Institutional ethical approval required
- Informed consent mandatory
Non-compliance leads to rejection.
12. Errata, Retractions & Corrections
FPR ensures integrity of scholarly record:
- Minor errors → corrigendum
- Major errors → retraction
- Misconduct → full withdrawal notice
All updates are clearly linked to original articles.
13. Digital Preservation Policy
The journal ensures long-term accessibility via:
- Digital archiving systems
- Repository storage
- Regular backups
14. Advertisement Policy
FPR maintains editorial independence.
- No misleading advertisements
- Ads (if any) are clearly separated
- No influence on editorial decisions
15. Editorial Policies
- Double-blind peer review
- Minimum 2 reviewers per article
- Decisions based on pharmacological and scientific merit
- No bias or discrimination
16. Conflict of Interest & Financial Disclosure
Authors must declare:
- Funding sources
- Sponsorships
- Financial relationships
Transparency is mandatory.
17. Participant Privacy & Consent
- Personal data must be anonymized
- Written consent required for identifiable information
- Ethical compliance mandatory
18. Data Sharing Policy
Authors are encouraged to:
- Share datasets publicly
- Provide supplementary materials
- Include a Data Availability Statement
Sensitive pharmacological and clinical data must be protected.





