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From providing publication process guidance to helping in each step throughout the publication process.
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Global Reach
Contact our experts at any time without any hesitation! It is because our customer support team will always be there to provide you with customised solutions catered to your needs.
Comprehensive Methodology
Provide transparent methodology for reproducibility while including descriptions of analytical tools, sampling methods, and experimental setups.
Insights Into Risk Management
Explore risk-based approaches in pharmaceutical manufacturing and supply chain management for drug quality research publication to make a strong impact with our support.
Insights Into Risk Management
Highlight practical applications, industry case studies, or collaborations between academia and industry in order to add substantial value to your articles.
Ethically Compliant
Adhere to ethical research practices with clear disclosure of approvals from regulatory and ethical bodies where applicable to meet the journal’s manuscript submission guidelines.
Technical Rigour
Improve the chances of your article’s drug quality assurance journal publishing by submitting technically sound content with clarity while explaining complex processes.Future Perspectives
Emerging Industry Challenges
Include insights into emerging challenges like AI-driven quality control, green manufacturing practices, or personalised medicine to enrich your content's relevance.
Pick the topics that address modern industry challenges by integrating digital tools like blockchain and AI in quality assurance frameworks.
Propose key performance indicators for measuring pharmaceutical quality at various stages of production to improve the calibre of your article.
This is how; our experts pick the most thought-provoking articles that critically assess the gaps and challenges that existing norms of the pharmaceutical quality systems with solid pieces of evidence.
No matter how intriguing or thoughtful your article’s data might be, but it will be useless if it isn’t in compliance with IJPQA guidelines. Our experts are well-versed with all the guidelines of the journal which they ensure to implement one-by-one in your content.
This is how; you get a chance to maximise your article’s chances of success in the International Journal of Pharmaceutical Quality Assurance with our expert support designed to meet every guideline.
Yes! Processing or publication fees might apply. Specific details can be found by consulting the journal's website or contacting the editorial office.
The journal follows a double-blind peer-review process, ensuring impartial evaluation of articles by field experts. Reviewers assess the manuscript's quality, originality, and relevance.
The IJPQA journal publishes research topics on pharmaceutical quality, analytical techniques, formulation development, regulatory affairs, Good Manufacturing Practices, and advancements in pharmaceutical quality assurance methodologies.
You can submit your research to IJPQA through the journal's official submission portal by adhering to the provided guidelines. Detailed instructions are available on the journal’s website.
The initial review process typically takes a few weeks, and publication may take several months. The timeline depends on reviewer availability and the required revisions.
Yes! The IJPQA journal offers open-access options, allowing broader dissemination of research. Authors can confirm specific open-access terms on the journal’s website.
Authors can access detailed submission guidelines and email support for queries regarding manuscript preparation, formatting, and submission.
Manuscripts must adhere to the IJPQA journal's formatting guidelines, including font style, spacing, citation style, and structure. Specific requirements are outlined in the author instructions section on the journal’s website.