Skip to content

Booksellers & Trade Customers: Sign up for online bulk buying at trade.atlanticbooks.com for wholesale discounts

Booksellers: Create Account on our B2B Portal for wholesale discounts

Volume 1: Comprehensive Guide to Pharmaceutical Regulatory Affairs: Principles and Practices

by Muralidhar Rao Akkaladevi , Veerareddy Prabhakar Reddy
Save 9% Save 9%
Current price ₹2,528.00
Original price ₹2,782.00
Original price ₹2,782.00
Original price ₹2,782.00
(-9%)
₹2,528.00
Current price ₹2,528.00

Imported Edition - Ships in 18-21 Days

Free Shipping in India on orders above Rs. 500

Request Bulk Quantity Quote
+91
Book cover type: Paperback
  • ISBN13: 9798895199244
  • Binding: Paperback
  • Subject: N/A
  • Publisher: Notion Press
  • Publisher Imprint: Notion Press
  • Publication Date:
  • Pages: 352
  • Original Price: GBP 21.99
  • Language: English
  • Edition: N/A
  • Item Weight: 635 grams
  • BISAC Subject(s): Research

Comprehensive Guide to Pharmaceutical Regulatory Affairs is an essential resource for anyone involved in the pharmaceutical industry, particularly those working in regulatory affairs. This book provides a thorough understanding of the principles and practices that ensure the safety, efficacy, and quality of pharmaceutical products.

It begins with Good Regulatory Practices, providing a strong foundation in the basic principles of regulatory affairs. Subsequent chapters delve into Good Laboratory Practices, Good Automated Laboratory Practices, and Good Distribution Practices, each offering detailed insights into maintaining high standards across different stages of pharmaceutical production and distribution.

The section on Quality Management Systems explores the implementation of effective quality assurance mechanisms, ensuring that all pharmaceutical products meet stringent quality standards. Detailed chapters on Documentation and Regulatory Writing, Dossier Preparation and Submission, and Audits offer practical guidance on the critical documentation processes and audit procedures required for regulatory approval and ongoing compliance.

The book also addresses the complexities of Inspections and Product Life Cycle Management, providing comprehensive guidance on maintaining compliance throughout the product lifecycle. A comprehensive List of Abbreviations and Acronyms and a detailed Bibliography serve as valuable reference tools, enhancing the utility of this guide.

Trusted for over 49 years

Family Owned Company

Secure Payment

All Major Credit Cards/Debit Cards/UPI & More Accepted

New & Authentic Products

India's Largest Distributor

Need Support?

Whatsapp Us