How to Develop Robust Scale-up Strategies for Complex Injectable Dosage Forms How to Develop Robust Scale-up Strategies for Complex Injectable Dosage Forms
Expertise in Pharmaceutical Process Technology

How to Develop Robust Scale-up Strategies for Complex Injectable Dosage Forms

From Bench to the Clinics

Neelam Poonia and Others
    • $179.99
    • $179.99

Publisher Description

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

GENRE
Professional & Technical
RELEASED
2026
February 16
LANGUAGE
EN
English
LENGTH
400
Pages
PUBLISHER
Academic Press
SELLER
Elsevier Ltd.
SIZE
43.3
MB
How to Optimize Fluid Bed Processing Technology How to Optimize Fluid Bed Processing Technology
2017
How to Integrate Quality by Efficient Design (QbED) in Product Development How to Integrate Quality by Efficient Design (QbED) in Product Development
2019
How to Design and Implement Powder-to-Tablet Continuous Manufacturing Systems How to Design and Implement Powder-to-Tablet Continuous Manufacturing Systems
2022
Principles of Parenteral Solution Validation Principles of Parenteral Solution Validation
2019
How to Scale-Up a Wet Granulation End Point Scientifically How to Scale-Up a Wet Granulation End Point Scientifically
2015