Asian Journal of Pharmaceutical Analysis

ISSN

2231-5675 (Online)
2231-5667 (Print)


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Correction and Retraction Policy


The Asian Journal of Pharmaceutical Analysis (AJPAna) is firmly committed to preserving the accuracy, reliability, and academic integrity of every article it publishes. Any corrections, updates, or retractions made whether on the AJPAna website or within already published manuscripts are carried out in strict accordance with the guidelines established by the Committee on Publication Ethics (COPE) for retractions and related editorial actions. By following these internationally recognized standards, AJPAna ensures that the scholarly record remains transparent, trustworthy, and ethically maintained.


Asian Journal of Pharmaceutical Analysis (AJPA) is an international, peer-reviewed journal, devoted to pharmaceutical analysis...... Read more >>>

RNI: Not Available                     
DOI: 10.5958/2231–5675 

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Integrated In-Silico Toxicological Risk Assessment of Vonoprazan Degradation Products using Complementary QSAR Approaches
Emerging and Established Methods for Cefepime Quantification: A Detailed Review
Contemporary Trends in Analytical Method Development for Dapagliflozin and Pioglitazone: A Critical Review of Spectroscopic and Chromatographic Approaches
Role of Forced Degradation in Stability Indicating Method Development: A Comprehensive Review
Simultaneous Estimation of Multicomponent Drugs by HPLC: A Comprehensive Review on Method Development and Validation
Development of Ion- pair Extractive Spectrophotometric Method for the determination of Ranolazine in Pharmaceutical Dosage Forms
Reverse Phase High Performance Liquid Chromatography Method for Simultaneous Estimation of Budesonide and Formoterol in Pure and Tablet
Isolation, Characterization and Purity Assessment of Caffeine from Commercial Tea Products
Development and Validation of Analytical Method for Estimation of Zinc and Manganese by Atomic Absorption Spectrophotometer in Multivitamin and Multimineral Syrup
Development and Validation of the NP-HPTLC Method for the Estimation of Dimenhydrinate in Bulk and Tablet Formulation
Eco-Friendly QbD-Driven RP-HPLC Method for Stability Analysis of Lamotrigine
Central Composite Design Aided Method Development and Validation of a Reverse Phase HPLC Method for Escitalopram in Synthetic Mixture
Analytical Method Development and Validation of Vadadustat in Bulk and Pharmaceutical Dosage Forms by Using RP-HPLC
A Novel RP-HPLC Method Development and Validation for Determination of Palbociclib drug in tablet Formulation
Analytical Quality by Design-Based RP-HPLC Method for Simultaneous Estimation of Lobeglitazone sulfate and Glimeperide in Pharmaceutical Formulations
Beyond Chromatograms: Green Analytical Frontiers in the Nutraceutical Era
Method Development and Validation for the Assay of the Anticoagulant dosage form by HPLC
Validation of the UV Spectrophotometric Method for the Quantitative measurement of Clopidogrel bisulphate in Pharmaceutical Dosage Form and Bulk
Analytical method development and validation for Simultaneous Estimation of Rifampicin and Levofloxacin in Bulk and Synthetic Mixtures Using Validated RP- HPLC Technique
A High-Precision RP–HPLC Method for Ondansetron Hydrochloride: Development, Optimization and Validation

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