Expertise in Pharmaceutical Process Technology – serie
Visar alla böcker i serien Expertise in Pharmaceutical Process Technology. Handla med fri frakt och snabb leverans.
8 produkter
How to Scale-Up a Wet Granulation End Point Scientifically
Häftad, 2015
536 kr
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How to Scale-Up a Wet Granulation End Point Scientifically provides a single-source devoted to all relevant information on the scale-up of a wet granulation end point. Contents include a general description, problem identification, and theoretical background with supporting literature, case …
How to Validate a Pharmaceutical Process
Häftad, 2016
496 kr
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How to Validate a Pharmaceutical Process provides a "how to� approach to developing and implementing a sustainable pharmaceutical process validation program. The latest volume in the Expertise in Pharmaceutical Process Technology Series, this book illustrates the methods and reasoning behind …
How to Optimize Fluid Bed Processing Technology
Part of the Expertise in Pharmaceutical Process Technology Series
Av Dilip Parikh
Häftad, 2017
681 kr
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How to Optimize Fluid Bed Processing Technology: Part of the Expertise in Pharmaceutical Process Technology Series addresses the important components of fluid bed granulation, providing answers to problems that commonly arise and using numerous practical examples and case studies as reference. This …
How to Develop Robust Solid Oral Dosage Forms
From Conception to Post-Approval
Häftad, 2016
681 kr
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How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval uses a practical and hands-on approach to cover the development process of solid oral dosage forms in one single source. The book details all of the necessary steps from formulation through the post-approval phase and …
Principles of Parenteral Solution Validation
A Practical Lifecycle Approach
Av Igor Gorsky, Harold S. Baseman
Häftad, 2019
1051 kr
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Principles of Parenteral Solution Validation: A Practical Lifecycle Approach covers all aspects involved in the development and process validation of a parenteral product. By using a lifecycle approach, this book discusses the latest technology, compliance developments, and regulatory …
How to Design and Implement Powder-to-Tablet Continuous Manufacturing Systems
Av Fernando Muzzio, Sarang Oka
Häftad, 2022
1238 kr
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How to Design and Implement Powder-to-Tablet Continuous Manufacturing Systems provides a comprehensive overview on the considerations necessary for the design of continuous pharmaceutical manufacturing processes. The book covers both the theory and design of continuous processing of associated unit …
How to Integrate Quality by Efficient Design (QbED) in Product Development
Häftad, 2019
1527 kr
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The development of a robust drug product requires juggling many competing priorities such as overcoming scientific challenges, following regulatory requirements, and managing business-related concerns. Unfortunately, despite large resources spent on R&D, multifactor productivity of pharmaceuticals …
How to Develop Robust Scale-up Strategies for Complex Injectable Dosage Forms
From Bench to the Clinics
Av Neelam Poonia, Jitender Madan m. fl.
Häftad, 2026
1831 kr
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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 …
