Journal of Pharma and Drug Regulatory Affairs

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About Us

The Journal of Pharma and Drug Regulatory Affairs is a peer-reviewed journal that provides a platform for publishing original research, review articles, and case studies in the field of pharmaceutical and drug regulatory affairs. It serves as a forum for researchers, academicians, regulatory professionals, and pharmaceutical industry experts to share knowledge, insights, and developments related to regulatory compliance, quality, safety, efficacy, and global regulatory standards. The journal covers areas including ICH/GCP, regulatory affairs, Good Manufacturing Practices (GMP), drug and biologics regulation, medical devices, biopharmaceutical regulations, Drug Master Files (DMF), regulatory dossiers, drug import and export, Ayurvedic regulations, and medical diagnostics.

Aim

JPDRA aims to provide a scholarly platform for researchers, academicians, scholars, and pharmaceutical professionals to disseminate high-quality research, reviews, and case studies in the field of drugs and pharmaceutical regulatory sciences.The journal promotes research and knowledge exchange in pharmaceutical regulatory affairs, drug development, manufacturing, quality, and compliance with national and international standards.JPDRA seeks to support advancements in regulatory science, pharmaceutical practices, biopharmaceuticals, medical devices, diagnostics, and related healthcare sectors.

Focus and Scope

ICH Guidelines and Good Clinical Practice (GCP) Pharmaceutical Regulatory Affairs Regulatory Affairs for Medical Devices Drug Manufacturing and Manufacturing Processes Import and Export of Drugs Biopharmaceutical Regulations Indian Pharmaceutical Regulations Good Manufacturing Practices (GMP) Drug Master File (DMF) Common Technical Document (CTD) and Regulatory Dossiers

Drug and Biologics Regulatory Affairs Ayurvedic and Traditional Medicine Regulations Medical Diagnostics and Diagnostic Regulations Pharmaceutical Quality and Compliance Drug Registration and Marketing Authorization Pharmacovigilance and Drug Safety Regulatory Science and Policy Clinical Research and Regulatory Compliance Medical Product Development and Regulation