• Home
  • How to Scale Up a Wet Granulation End Point Scientifically

How to Scale Up a Wet Granulation End Point Scientifically

How to Scale Up a Wet Granulation End Point Scientifically
  • Author : Michael Levin
  • Publsiher : Academic Press
  • Release : 07 October 2015
  • ISBN : 0128035609
  • Pages : 88 pages
  • Rating : 4/5 from 21 ratings
GET THIS BOOKHow to Scale Up a Wet Granulation End Point Scientifically

Summary:
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 studies, potential solutions, and more. By outlining issues related to scale-up and end-point determination, and then using practical examples and advice to address these issues, How to Scale-Up a Wet Granulation End Point Scientifically is a valuable and essential resource for all those pharmaceutical scientists and technologists engaged in the granulation process. Thoroughly referenced and based on the latest research and literature Part of the Expertise in Pharmaceutical Process Technology Series edited by internationally respected expert, Michael Levin Illustrates the most common problems related to scale-up of a wet granulation end point and provides valuable insights on how to solve these problems in a practical way


How to Scale-Up a Wet Granulation End Point Scientifically

How to Scale-Up a Wet Granulation End Point Scientifically
  • Author : Michael Levin
  • Publisher : Academic Press
  • Release : 07 October 2015
GET THIS BOOKHow to Scale-Up a Wet Granulation End Point Scientifically

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 studies, potential solutions, and more. By outlining issues related to scale-up and end-point determination, and then using practical examples and advice to address these issues, How to Scale-Up a Wet Granulation End Point Scientifically is a valuable and essential resource

Book How to Scale-Up a Wet Granulation End Point Scientifically PDF Download/ Read Online



Handbook of Pharmaceutical Wet Granulation

Handbook of Pharmaceutical Wet Granulation
  • Author : Ajit S. Narang,Sherif I.F. Badawy
  • Publisher : Academic Press
  • Release : 31 August 2018
GET THIS BOOKHandbook of Pharmaceutical Wet Granulation

Handbook of Pharmaceutical Wet Granulation: Theory and Practice in a Quality by Design Paradigm offers a single and comprehensive reference dedicated to all aspects of pharmaceutical wet granulation, taking a holistic approach by combining introductory principles with practical solutions. Chapters are written by international experts across industry, academic and regulatory settings, and cover a wide spectrum of relevant and contemporary wet granulation topics, techniques and processes. The books' focus on process analytical technology, quality by design principles, granulation equipment, modeling,

Book Handbook of Pharmaceutical Wet Granulation PDF Download/ Read Online


Dosage Form Design Considerations

Dosage Form Design Considerations
  • Author : Anonim
  • Publisher : Academic Press
  • Release : 28 July 2018
GET THIS BOOKDosage Form Design Considerations

Dosage Form Design Parameters, Volume I, examines the history and current state of the field within the pharmaceutical sciences, presenting key developments. Content includes drug development issues, the scale up of formulations, regulatory issues, intellectual property, solid state properties and polymorphism. Written by experts in the field, this volume in the Advances in Pharmaceutical Product Development and Research series deepens our understanding of dosage form design parameters. Chapters delve into a particular aspect of this fundamental field, covering principles, methodologies

Book Dosage Form Design Considerations PDF Download/ Read Online


How to Integrate Quality by Efficient Design (QbED) in Product Development

How to Integrate Quality by Efficient Design (QbED) in Product Development
  • Author : Bhavishya Mittal
  • Publisher : Academic Press
  • Release : 24 August 2019
GET THIS BOOKHow to Integrate Quality by Efficient Design (QbED) in Product Development

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 is on the decline for several years now. Because of this business reality, pharmaceutical companies have seen a notable change in the traditional operating model and footprint over the past couple of decades. Outsourcing, in particular, has emerged as a successful business model for

Book How to Integrate Quality by Efficient Design (QbED) in Product Development PDF Download/ Read Online


How to Develop Robust Solid Oral Dosage Forms

How to Develop Robust Solid Oral Dosage Forms
  • Author : Bhavishya Mittal
  • Publisher : Academic Press
  • Release : 05 October 2016
GET THIS BOOKHow to Develop Robust Solid Oral Dosage Forms

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 contains industry case studies, real world advice, and troubleshooting tips. By merging the latest scientific information with practical instructions, this book provides pharmaceutical scientists in formulation research and development with a concrete look

Book How to Develop Robust Solid Oral Dosage Forms PDF Download/ Read Online


How to Optimize Fluid Bed Processing Technology

How to Optimize Fluid Bed Processing Technology
  • Author : Dilip Parikh
  • Publisher : Academic Press
  • Release : 04 April 2017
GET THIS BOOKHow to Optimize Fluid Bed Processing Technology

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 book covers the theoretical concepts involved in fluidization, also providing a description of the choice and functionality of equipment. Additional chapters feature key aspects of the technology, including formulation requirements, process variables, process scale-up, troubleshooting, new development, safety,

Book How to Optimize Fluid Bed Processing Technology PDF Download/ Read Online


Principles of Parenteral Solution Validation

Principles of Parenteral Solution Validation
  • Author : Igor Gorsky,Harold S. Baseman
  • Publisher : Academic Press
  • Release : 15 April 2019
GET THIS BOOKPrinciples of Parenteral Solution Validation

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 considerations and trends, from process design, to divesting. As part of the Expertise in Pharmaceutical Process Technology series edited by Michael Levin, this book incorporates numerous case studies and real-world examples that address timely problems and offer solutions to the daily challenges

Book Principles of Parenteral Solution Validation PDF Download/ Read Online


Current Trends and Future Developments on (Bio-) Membranes

Current Trends and Future Developments on (Bio-) Membranes
  • Author : Angelo Basile,Alberto Figoli,Yongdan Li
  • Publisher : Elsevier
  • Release : 27 November 2019
GET THIS BOOKCurrent Trends and Future Developments on (Bio-) Membranes

Current Trends and Future Developments in (Bio-) Membranes: Membranes in Environmental Applications offers an overview of environmental pollution, covering the air, water, waste from agriculture and climate change, and including emerging offenders such as microplastics and electronic waste which can be solved by conventional and advanced membrane techniques. Chapters cover environmental pollution issues followed by specific membrane processes, problems related to environmental pollution, and the different techniques used for solving these problems. For each pollutant, such as CO2 and fuel,

Book Current Trends and Future Developments on (Bio-) Membranes PDF Download/ Read Online


Chemical Engineering in the Pharmaceutical Industry

Chemical Engineering in the Pharmaceutical Industry
  • Author : Mary T. am Ende,David J. am Ende
  • Publisher : John Wiley & Sons
  • Release : 08 April 2019
GET THIS BOOKChemical Engineering in the Pharmaceutical Industry

A guide to the important chemical engineering concepts for the development of new drugs, revised second edition The revised and updated second edition of Chemical Engineering in the Pharmaceutical Industry offers a guide to the experimental and computational methods related to drug product design and development. The second edition has been greatly expanded and covers a range of topics related to formulation design and process development of drug products. The authors review basic analytics for quantitation of drug product quality

Book Chemical Engineering in the Pharmaceutical Industry PDF Download/ Read Online


Developing Solid Oral Dosage Forms

Developing Solid Oral Dosage Forms
  • Author : Yihong Qiu,Yisheng Chen,Geoff G.Z. Zhang,Lirong Liu,William Porter
  • Publisher : Academic Press
  • Release : 10 March 2009
GET THIS BOOKDeveloping Solid Oral Dosage Forms

Developing Solid Oral Dosage Forms is intended for pharmaceutical professionals engaged in research and development of oral dosage forms. It covers essential principles of physical pharmacy, biopharmaceutics and industrial pharmacy as well as various aspects of state-of-the-art techniques and approaches in pharmaceutical sciences and technologies along with examples and/or case studies in product development. The objective of this book is to offer updated (or current) knowledge and skills required for rational oral product design and development. The specific goals

Book Developing Solid Oral Dosage Forms PDF Download/ Read Online


Continuous Manufacturing of Pharmaceuticals

Continuous Manufacturing of Pharmaceuticals
  • Author : Peter Kleinebudde,Johannes Khinast,Jukka Rantanen
  • Publisher : John Wiley & Sons
  • Release : 14 July 2017
GET THIS BOOKContinuous Manufacturing of Pharmaceuticals

A comprehensive look at existing technologies and processes for continuous manufacturing of pharmaceuticals As rising costs outpace new drug development, the pharmaceutical industry has come under intense pressure to improve the efficiency of its manufacturing processes. Continuous process manufacturing provides a proven solution. Among its many benefits are: minimized waste, energy consumption, and raw material use; the accelerated introduction of new drugs; the use of smaller production facilities with lower building and capital costs; the ability to monitor drug quality

Book Continuous Manufacturing of Pharmaceuticals PDF Download/ Read Online


Pharmaceutical Blending and Mixing

Pharmaceutical Blending and Mixing
  • Author : P. J. Cullen,Rodolfo J. RomaƱach,Nicolas Abatzoglou,Chris D. Rielly
  • Publisher : John Wiley & Sons
  • Release : 11 May 2015
GET THIS BOOKPharmaceutical Blending and Mixing

Written in four parts, this book provides a dedicated and in-depth reference for blending within the pharmaceutical manufacturing industry. It links the science of blending with regulatory requirements associated with pharmaceutical manufacture. The contributors are a combination of leading academic and industrial experts, who provide an informed and industrially relevant perspective of the topic. This is an essential book for the pharmaceutical manufacturing industry, and related academic researchers in pharmaceutical science and chemical and mechanical engineering.

Book Pharmaceutical Blending and Mixing PDF Download/ Read Online


Oral Controlled Release Formulation Design and Drug Delivery

Oral Controlled Release Formulation Design and Drug Delivery
  • Author : Hong Wen,Kinam Park
  • Publisher : John Wiley & Sons
  • Release : 14 January 2011
GET THIS BOOKOral Controlled Release Formulation Design and Drug Delivery

This book describes the theories, applications, and challenges for different oral controlled release formulations. This book differs from most in its focus on oral controlled release formulation design and process development. It also covers the related areas like preformulation, biopharmaceutics, in vitro-in vivo correlations (IVIVC), quality by design (QbD), and regulatory issues.

Book Oral Controlled Release Formulation Design and Drug Delivery PDF Download/ Read Online


Integrated Pharmaceutics

Integrated Pharmaceutics
  • Author : Antoine Al-Achi,Mali Ram Gupta,William Craig Stagner
  • Publisher : John Wiley & Sons
  • Release : 11 February 2013
GET THIS BOOKIntegrated Pharmaceutics

Focusing on the application of physical pharmacy, drug design, and drug regulations as they relate to produce effective dosage forms for drug delivery, Integrated Pharmaceutics provides a comprehensive picture of pharmaceutical product design, describing the science and art behind the concepts of dosage form development. Combining physical pharmacy, product design, and regulatory affairs issues in a single book, the authors address topics governing drug regulations of United States, European, and Japanese agencies and detail new regulatory guidelines, including quality by

Book Integrated Pharmaceutics PDF Download/ Read Online