Regulatory Affairs in Pharmacy: Policies, Compliance, and Global Perspectives

In today’s rapidly evolving healthcare landscape, the role of regulatory affairs in pharmacy has become increasingly critical. With the globalization of the pharmaceutical industry, the complexity of drug development, and the growing demand for safe and effective medicines, regulatory affairs professionals must navigate a multifaceted landscape of policies, guidelines, and compliance requirements that vary across regions and markets. Effective regulation ensures the safety, efficacy, and quality of pharmaceutical products, from discovery to patient use, making it central to public health and global healthcare systems.
Regulatory Affairs in Pharmacy: Policies, Compliance, and Global Perspectives seeks to provide a comprehensive and insightful overview of the regulatory frameworks that govern the pharmaceutical industry, focusing on the policies, processes, and global considerations that shape the industry today. This book explores the evolving role of regulatory affairs in ensuring compliance with safety standards, promoting public health, and facilitating the approval and availability of new treatments.
This book is intended for professionals in regulatory affairs, pharmaceutical industry experts, healthcare policymakers, and students of pharmacy and pharmaceutical sciences. By offering both theoretical insights and practical strategies, Regulatory Affairs in Pharmacy provides a valuable resource for those seeking to understand the dynamic relationship between regulatory policies, compliance, and the global pharmaceutical market.
We hope that this work fosters a deeper understanding of the critical role regulatory affairs plays in advancing public health and encourages continued collaboration and innovation within the pharmaceutical sector, ensuring that safe and effective treatments reach patients worldwide.