Submit Your Pharmaceutical Research to JAPST
Join leading pharmaceutical scientists publishing breakthrough research in drug formulation, delivery systems, and pharmaceutical technology
Two Convenient Ways to Submit Your Manuscript
Choose the submission method that works best for your research workflow. Both options provide secure, efficient manuscript handling with full tracking capabilities.
ManuscriptZone Portal
Our comprehensive manuscript management system designed for pharmaceutical research submissions. Ideal for complex formulation studies, multi-author collaborations, and manuscripts with extensive supplementary data.
- Auto-save functionality protects your work
- Real-time submission status tracking
- Direct communication with reviewers and editors
- Secure file upload for large datasets and high-resolution images
- Guided workflow ensures completeness
- Access reviewer comments and revision requests instantly
Quick Submission Form
Streamlined submission process for straightforward pharmaceutical research papers. Perfect for short communications, rapid reports, and single-author manuscripts.
- No account registration required
- Simple one-page submission form
- Fast upload for standard manuscript formats
- Immediate confirmation email
- Ideal for time-sensitive submissions
- Seamless transition to full portal if needed
Pharmaceutical Research We Publish
JAPST specializes in publishing cutting-edge pharmaceutical science and technology research. Our expert reviewers understand the complexities of drug development, formulation science, and pharmaceutical engineering.
Original Research Articles
Novel drug formulation studies, nanoparticle delivery systems, controlled release mechanisms, bioavailability enhancement, and pharmaceutical material characterization.
Pharmaceutical Technology Methods
Innovative analytical techniques, quality control methodologies, stability testing protocols, dissolution studies, and pharmaceutical process optimization.
Drug Delivery Systems
Targeted delivery platforms, transdermal systems, oral formulations, injectable depot systems, and novel carrier technologies for pharmaceutical applications.
Pharmacokinetic Studies
ADME studies, bioequivalence research, pharmacokinetic modeling, drug-drug interactions, and population pharmacokinetics in pharmaceutical development.
Pharmaceutical Biotechnology
Biopharmaceutical formulation, protein stability, biologics delivery, biosimilar development, and biotechnology applications in drug manufacturing.
Rapid Communications
Preliminary formulation findings, breakthrough delivery technologies, urgent pharmaceutical safety data, and time-sensitive pharmaceutical research.
Review Articles
Comprehensive reviews of pharmaceutical technologies, drug delivery trends, formulation strategies, regulatory perspectives, and emerging pharmaceutical sciences.
Case Studies
Formulation problem-solving, scale-up challenges, stability issues, regulatory case studies, and real-world pharmaceutical development experiences.
Pre-Submission Checklist for Pharmaceutical Research
Ensure your pharmaceutical manuscript meets our quality standards before submission. This checklist helps pharmaceutical scientists prepare comprehensive, publication-ready research.
Word (.docx) or LaTeX format with all sections complete: Abstract, Introduction, Materials & Methods, Results, Discussion, Conclusion
High-resolution images (300 DPI minimum), TIFF or EPS format for graphs, clear labeling of formulation data, dissolution profiles, and analytical results
All formulation compositions disclosed, analytical methods validated, stability data included, statistical analysis performed
IRB approval for human studies, IACUC approval for animal studies, ethics committee documentation ready for upload
Author list finalized, affiliations accurate, corresponding author designated, all co-authors approved submission
Financial relationships disclosed, pharmaceutical industry funding acknowledged, potential conflicts identified
All citations checked, pharmaceutical databases referenced (PubMed, SciFinder), reference style consistent throughout
Raw analytical data, additional formulation details, extended stability studies, supplementary figures prepared
Pharmaceutical Research Tip: Include detailed formulation compositions, manufacturing processes, and analytical validation data. Our reviewers are pharmaceutical scientists who appreciate comprehensive methodology and reproducible protocols. Clear documentation of excipient grades, processing parameters, and quality control measures strengthens your manuscript.
Your Manuscript's Journey: From Submission to Publication
Transparent, efficient peer review by pharmaceutical science experts. Every step designed to provide constructive feedback and maintain the highest standards of pharmaceutical research publishing.
Submission & Initial Screening
Your pharmaceutical manuscript is received and checked for completeness, formatting compliance, and scope alignment. Plagiarism screening via iThenticate ensures originality. Manuscripts with clear pharmaceutical science focus proceed immediately.
3 daysEditor Assignment
A pharmaceutical science editor with expertise in your specific area (formulation, delivery systems, pharmacokinetics, etc.) is assigned. The editor reviews your manuscript and selects appropriate peer reviewers from our network of pharmaceutical scientists.
3-5 daysExpert Peer Review
Typically 2-3 pharmaceutical scientists with relevant expertise review your manuscript. They evaluate formulation design, analytical methods, data interpretation, pharmaceutical significance, and reproducibility. Constructive feedback focuses on strengthening your research.
21 daysEditorial Decision
Based on reviewer recommendations, the editor makes a decision: Accept, Minor Revisions, Major Revisions, or Reject. You receive detailed reviewer comments and specific guidance for revisions. Our 40% acceptance rate reflects rigorous quality standards.
28 days totalRevision & Re-review
If revisions are requested, you submit your revised manuscript with a detailed response to reviewers. Pharmaceutical editors appreciate point-by-point responses addressing each comment. Revised manuscripts undergo expedited re-review by the same experts.
14 daysAcceptance & Production
Upon acceptance, your manuscript enters production. Professional copyediting, XML conversion, DOI assignment, and final proofing ensure publication quality. Your pharmaceutical research is prepared for global dissemination.
10 daysPublication & Indexing
Your article is published online with immediate Open Access. Automatic submission to pharmaceutical databases ensures maximum visibility among pharmaceutical scientists, formulators, and drug development professionals worldwide.
ImmediateAverage Timeline: From submission to publication in approximately 60 days for manuscripts accepted without major revisions. Fast-track review available for breakthrough pharmaceutical technologies and urgent drug safety communications.
Why Pharmaceutical Scientists Choose JAPST
Expert Pharmaceutical Reviewers
Peer review by formulation scientists, pharmaceutical engineers, and drug delivery experts
Fast Decisions
Average 21 days to first decision, 14-day fast-track for rapid communications
Global Open Access
Immediate worldwide visibility, no subscription barriers, maximum research impact
APC Waivers Available
Financial support for eligible pharmaceutical researchers from developing countries
What Makes Pharmaceutical Research Successful at JAPST
We Prioritize Manuscripts That:
- Present novel formulation strategies with clear advantages over existing approaches, supported by comprehensive characterization data
- Demonstrate rigorous pharmaceutical methodology including validated analytical techniques, appropriate statistical analysis, and reproducible protocols
- Address significant pharmaceutical challenges such as poor bioavailability, stability issues, targeted delivery, or manufacturing scalability
- Provide detailed experimental procedures allowing other pharmaceutical scientists to reproduce your formulations and analytical methods
- Include thorough characterization of pharmaceutical systems: particle size, morphology, drug release kinetics, stability profiles, and quality attributes
- Discuss pharmaceutical implications of findings for drug development, formulation optimization, or clinical translation
- Reference relevant pharmaceutical literature and position work within current pharmaceutical science context
Pharmaceutical Research Areas We Emphasize:
- Nanoparticle drug delivery systems and nanomedicine formulations
- Controlled and sustained release technologies
- Bioavailability enhancement strategies and solubility improvement
- Transdermal and topical delivery systems
- Oral solid dosage form development and optimization
- Injectable formulations and parenteral drug delivery
- Pharmaceutical materials science and excipient functionality
- Drug stability studies and degradation kinetics
- Pharmaceutical analysis and quality control methods
- Pharmacokinetic modeling and ADME studies
- Biopharmaceutics and drug absorption mechanisms
- Pharmaceutical process development and scale-up
Preparing Your Pharmaceutical Manuscript
Essential Components for Pharmaceutical Research Papers:
Title: Should clearly indicate the pharmaceutical focus (e.g., "Development and Characterization of Chitosan-Based Nanoparticles for Oral Delivery of Poorly Soluble Drugs" rather than generic "Novel Drug Delivery System")
Abstract: Structure with Background (pharmaceutical problem), Methods (formulation approach), Results (key findings with data), and Conclusion (pharmaceutical significance). Include quantitative results (e.g., "increased bioavailability by 3.2-fold" not just "improved bioavailability")
Materials & Methods: Provide complete formulation compositions with exact quantities, grades of pharmaceutical excipients, manufacturing procedures with process parameters, and validated analytical methods with acceptance criteria. This section should enable reproducibility by other pharmaceutical scientists.
Results: Present pharmaceutical data systematically: formulation characterization, in vitro release studies, stability data, and pharmacokinetic parameters if applicable. Use appropriate statistical analysis and clearly label all figures showing dissolution profiles, particle size distributions, or analytical chromatograms.
Discussion: Interpret findings in pharmaceutical context, compare with existing formulation approaches, discuss limitations and advantages, and suggest future pharmaceutical applications or clinical translation potential.
Ready to Share Your Pharmaceutical Research?
Join pharmaceutical scientists worldwide who trust JAPST for publishing their formulation studies, drug delivery innovations, and pharmaceutical technology advances.
Submit Your Manuscript NowNeed assistance with your submission? Our editorial team is here to help: [email protected]
