Regulatory Aspects of Pharmaceutical Quality System – Brief Introduction

If you're a B. Pharm or M. Pharm student seeking a comprehensive yet concise guide to the regulatory aspects of pharmaceutical quality systems look no further than Regulatory Aspects of Pharmaceutical Quality System – Brief Introduction. While other textbooks on quality assurance cover a variety of topics to varying degrees of depth this book provides a unified approach that is both insightful and practical. Designed to meet the needs of modern students and instructors this book covers the basic guidelines and principles of quality assurance as they relate specifically to drug design development and evaluation. You'll learn about the latest developments in the industry and how to apply these principles to the real-world challenges that you're likely to encounter. Whether you're a seasoned pharmaceutical professional or just starting out you'll find this book to be an invaluable resource that you'll refer to time and time again.Contents:1.    Introduction to Quality Management System2.    Good Manufacturing Practice Regulations- A Brief Scenario3.    Pharmaceutical Quality System-An Overview to ICH Q10 Guidelines4.    Analysis of Corrective and Preventive Action5.    Assuring Pharmaceutical Quality-A Brief Analysis of SOP’s6.    Quality Defects-Achieving Zero Defects Policy7.    Handling of Market Complaints and Recalls Review of FDA-483 Form8.    Pharmaceutical Quality Audits9.    USFDA Guidelines-Process Validation10. Drug approval Process in India11. Regulatory Requirements for Dossier Filing in ROW and International Markets