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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.
