How to Develop Robust Scale-up Strategies for Complex Injectable Dosage Forms: From Bench to the Clinics (Expertise in Pharmaceutical Process Technology) (PDF)

by Neelam Poonia PhD (ed.), Jitender Madan PhD (ed.), Deepti Pandita PhD (ed.)

How to Develop Robust Scale-up Strategies for Complex Injectable Dosage Forms: From Bench to the Clinics provides a comprehensive roadmap for transitioning complex injectable formulations from the laboratory to clinical applications. Offering an exploration of various complex injectables, including liposomal dosage forms, nanoparticles, and microspheres, this book delves into dosage form design, excipient selection, stability studies, and optimization techniques. The book examines manufacturing technologies such as aseptic processing, sterile filtration, and lyophilization, and their applications in producing complex injectables. Discussions on quality control measures, analytical techniques, and quality assurance practices are provided to ensure consistent quality and purity throughout the manufacturing process.
Readers will benefit from the expert knowledge and practical insights shared by industry professionals and leading researchers, including successful examples of marketed complex injectables. Highlighting best practices and regulatory requirements, this book offers a comprehensive overview of the guidelines for the development, manufacturing, and commercialization of complex injectables. Ideal for pharmaceutical scientists, formulation developers, and regulatory professionals, this book is a valuable resource for anyone involved in the scale-up and commercialization of complex injectable dosage forms.

Provides comprehensive guidance on scaling-up complex injectables from lab to clinical applications
Offers in-depth insights into dosage form design, excipient selection, and stability studies
Explores advanced manufacturing technologies and quality control measures for consistent product quality
Highlights regulatory requirements and best practices for compliance with GMP and regulatory submissions
Includes successful examples and practical insights from industry experts and leading researchers