Journal of Advances in Bio- pharmaceutics and Pharmacovigilance

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About Us

The Journal of Advances in Biopharmaceutics and Pharmacovigilance is a peer-reviewed journal that provides a platform for publishing original research, review articles, case reports, technical contributions, and scholarly perspectives in the fields of biopharmaceutics, pharmacovigilance, drug safety, adverse drug reactions, and medication toxicity. It serves as a forum for scientists, academicians, researchers, pharmaceutical professionals, clinicians, regulatory experts, and industry practitioners to share knowledge, innovations, technologies, and developments related to the safe and effective use of medicines. The journal covers areas including clinical research, drug safety, pharmacovigilance systems, regulatory frameworks, signal detection, safety monitoring, adverse drug reactions, medication toxicity, and compliance practices, with emphasis on the safe, effective, and rational use of medicines and the protection of public health.

Aim

JABPP aims to provide a scholarly platform for scientists, academicians, researchers, pharmaceutical professionals, clinicians, regulatory experts, and industry practitioners to disseminate innovative research and scientific knowledge in pharmacovigilance and pharmaceutical safety. The journal promotes interdisciplinary research encompassing clinical research, adverse drug reactions, medication toxicity, drug safety monitoring, signal detection, pharmacovigilance compliance and management, regulatory guidelines, and post-marketing surveillance. JABPP seeks to advance pharmaceutical safety research by facilitating the exchange of high-quality scientific and clinical findings that support the identification, assessment, prevention, and management of risks associated with medicines and pharmaceutical interventions.

Focus and Scope

Clinical Research Pharmacovigilance Drug Safety Adverse Drug Reactions (ADRs) Adverse Drug Events Medication Side Effects Medication Toxicity Drug Safety Monitoring Post-Marketing Surveillance Signal Detection

Signal Management Pharmacovigilance Compliance and Management Risk Management and Risk Minimization Benefit–Risk Assessment Pharmacovigilance Regulations and Guidelines USFDA and European Union Regulatory Frameworks Clinical Safety Assessment Medication Error and Medication Safety Case Reports and Case Series Clinical Safety Data