Journal of Pharmaceutical Quality Assurance and Quality Control

Editorial Board Members Current Archives 1 Archives 2 Author Guidelines Editor Guidelines Login

About Us

The Journal of Pharmaceutical Quality Assurance and Quality Control is a peer-reviewed journal that provides a platform for publishing original research, review articles, technical contributions, and scholarly perspectives in the fields of pharmaceutical quality assurance and quality control. It serves as a forum for scientists, academicians, researchers, industry professionals, and quality experts to share knowledge, innovations, technologies, and developments related to pharmaceutical quality systems and practices. The journal covers areas including regulatory standards, quality management systems, pharmaceutical manufacturing practices, analytical procedures, quality assurance, quality control, compliance frameworks, and emerging developments, with emphasis on maintaining the quality, safety, efficacy, and consistency of pharmaceutical products.

Aim

JPQAQC aims to provide a scholarly platform for scientists, academicians, researchers, pharmaceutical professionals, quality experts, and industry practitioners to disseminate innovative research and scientific knowledge in pharmaceutical quality assurance and quality control. The journal promotes interdisciplinary research encompassing pharmaceutical manufacturing, quality management systems, analytical methods, validation, regulatory compliance, Good Manufacturing Practices, laboratory practices, auditing, and quality risk management. JPQAQC seeks to advance pharmaceutical quality research by facilitating the exchange of high-quality scientific and technical findings that contribute to the development, evaluation, monitoring, and continuous improvement of pharmaceutical products, processes, and quality systems.

Focus and Scope

Pharmaceutical Quality Assurance Pharmaceutical Quality Control Quality Management Systems Good Manufacturing Practices (GMP) Good Laboratory Practices (GLP) Quality Risk Management Regulatory Affairs and Compliance Pharmaceutical Manufacturing Process and Product Validation Analytical Method Development and Validation

Pharmaceutical Analysis Instrumental and Analytical Techniques Stability Studies and Stability Testing Pharmaceutical Microbiology Sterility Assurance and Testing Cleaning Validation Computer System Validation Standard Operating Procedures (SOPs) Auditing and Regulatory Inspection ISO Guidelines and Standards