The journal offers wide coverage of topics including trends and guidelines of various National and International regulatory agencies, Pharmacovigilance, new drug application processes, protocols of achieving regulatory compliance, legislative revisions, regulatory approvals, marketing practices, as well as the formulation & streamlining of the good manufacturing practice. The journal’s core focus is on the procedures, protocols, standards & policies, pharmaceutical regulations, quality control, and quality assurance of drug development.
The Pharmaceutical Regulatory Affairs: Open Access provides a unique platform to researchers and scientist to explore the advanced and latest research developments in the field of pharmaceutical regulatory affairs, thus bridging the gap between researchers and young scientists