Comprehensive Guide to Pharmaceutical Regulatory Science

<p><b>Comprehensive Guide to Pharmaceutical Regulatory Science</b> is an essential textbook designed to provide pharmaceutical professionals students and researchers with a deep understanding of regulatory science in the pharmaceutical industry. This book covers a wide range of topics including drug discovery clinical trials regulatory approval processes and post-market surveillance.&nbsp;</p><p><b>Key Features:</b></p><p><b>In-depth Coverage</b>: Learn about the complete regulatory landscape including the stages of drug discovery and development clinical trials regulatory approval processes (NDA IND ANDA) and international guidelines (FDA EMA ICH).</p><p><br/><b>Authoritative Insights:</b> Authored by renowned professionals with over 30 years of combined experience in pharmaceutical education regulatory affairs and pharmaceutical biotechnology.</p><p><br/><b>Global Perspective:</b> Detailed insights into the regulatory frameworks of the US EU Japan Canada and India with practical applications for professionals working in these regions.<br/>Real-World Applications: Understand the complexities of pharmaceutical regulation and how to navigate the approval process for drug products in various international markets.<br/>Perfect for Professionals & Students: This book is ideal for students pursuing B.Pharm M.Pharm PhD in pharmaceutical sciences and for professionals seeking to deepen their knowledge of pharmaceutical regulatory practices.<br/><br/><br/></p>