How to Develop Robust Scale-up Strategies for Complex Injectable Dosage Forms: From Bench to the Clinics is an essential guide providing a comprehensive roadmap for transitioning complex injectable formulations from the laboratory to clinical applications. Offering an in-depth exploration of various complex injectables, including liposomal dosage forms, nanoparticles, and microspheres, this book delves into the principles of dosage form design, excipient selection, stability studies, and optimization techniques. Readers will gain valuable insights into ensuring the stability, efficacy, and safety of injectables during the scale-up process, as well as strategies for maintaining product quality and consistency from lab-scale to commercial-scale production. The book thoroughly examines manufacturing technologies such as aseptic processing, sterile filtration, and lyophilization, and their applications in producing complex injectables. Detailed discussions on quality control measures, analytical techniques, and quality assurance practices are provided to ensure the consistent quality and purity of injectables 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. Discussions on Good Manufacturing Practices (GMP) and regulatory submissions underscore the importance of compliance in achieving successful product development. 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.
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Dr. Poonia has over 13 years of teaching and research experience. She has supervised 13 post-graduate research projects. She has 17 publications in national and international journals of repute and book chapters to her credit with a h and i-10 index of 10 and 11, respectively. She has also presented her research at various national and international conferences. Dr. Poonia has been working on the development of targeted nanosystems for delivery of anticancer agents. Her key areas of research include development of nanotechnology-based drug delivery systems viz. solid lipid nanoparticles, nanostructured lipid carriers, mesoporous silica nanoparticles, etc. for combating solubility, stability, toxicity and
MDR-related issues associated with drugs.Dr. Deepti Pandita is Professor in the Department of Pharmaceutics, DIPSAR, Delhi Pharmaceutical Science and Research University (DPSRU), New Delhi. She is Coordinator, Centre for Advanced Formulation and Technology (CAFT), a DSIR funded Centre; Coordinator, PhD Programme of DPSRU. Dr. Pandita has 20+ years of teaching and research experience, and previously was FCT Postdoctoral Fellow at University of Madeira, Portugal. Her key areas of research include nanomedicine & nanotheranostics, formulation development, drug discovery & repurposing, nano-mediated targeted delivery of phytochemicals.
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
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Paperback. Etat : new. Paperback. 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. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability. N° de réf. du vendeur 9780443403668
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