Design and Manufacture of Pharmaceutical Tablets

Design and Manufacture of Pharmaceutical Tablets offers real world solutions and outcomes of formulation and processing challenges of pharmaceutical tablets. This book includes numerous practical examples related to actual formulations that have been validated and marketed and covers important data in the areas of stability, dissolution, bioavailibity and processing. It provides important background and theoretical information on design and manufacturing and includes a full section dedicated to design experimental methodology and statistics. In addition, this book offers a a general discussion of excipients used in proper tablet design along with practical examples related to excipients. Drug development scientists in industry and academia, as well as students in the pharmaceutical sciences will greatly benefit from the practical knowledge and case examples provided throughout this book. Incorporates important mathematical models and computational applications Includes unique content on central composite design and augmented simplex lattice Provides background on important design principles with emphasis on quality-based design (QBD) of pharmaceutical dosage forms

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  • Author : Reynir Eyjolfsson
  • Publisher : Academic Press
  • Pages : 68 pages
  • ISBN : 012802187X
  • Rating : 4/5 from 21 reviews
CLICK HERE TO GET THIS BOOKDesign and Manufacture of Pharmaceutical Tablets

Design and Manufacture of Pharmaceutical Tablets

Design and Manufacture of Pharmaceutical Tablets
  • Author : Reynir Eyjolfsson
  • Publisher : Academic Press
  • Release : 15 October 2014
GET THIS BOOKDesign and Manufacture of Pharmaceutical Tablets

Design and Manufacture of Pharmaceutical Tablets offers real world solutions and outcomes of formulation and processing challenges of pharmaceutical tablets. This book includes numerous practical examples related to actual formulations that have been validated and marketed and covers important data in the areas of stability, dissolution, bioavailibity and processing. It provides important background and theoretical information on design and manufacturing and includes a full section dedicated to design experimental methodology and statistics. In addition, this book offers a a general

Pharmaceutical Dosage Forms - Tablets

Pharmaceutical Dosage Forms - Tablets
  • Author : Larry L. Augsburger,Stephen W. Hoag
  • Publisher : CRC Press
  • Release : 19 April 2016
GET THIS BOOKPharmaceutical Dosage Forms - Tablets

The ultimate goal of drug product development is to design a system that maximizes the therapeutic potential of the drug substance and facilitates its access to patients. Pharmaceutical Dosage Forms: Tablets, Third Edition is a comprehensive resource of the design, formulation, manufacture, and evaluation of the tablet dosage form, an

Essential Chemistry for Formulators of Semisolid and Liquid Dosages

Essential Chemistry for Formulators of Semisolid and Liquid Dosages
  • Author : Vitthal S. Kulkarni,Charles Shaw
  • Publisher : Academic Press
  • Release : 15 October 2015
GET THIS BOOKEssential Chemistry for Formulators of Semisolid and Liquid Dosages

A needed resource for pharmaceutical scientists and cosmetic chemists, Essential Chemistry for Formulators of Semisolid and Liquid Dosages provides insight into the basic chemistry of mixing different phases and test methods for the stability study of nonsolid formulations. The book covers foundational surface/colloid chemistry, which forms the necessary background for making emulsions, suspensions, solutions, and nano drug delivery systems, and the chemistry of mixing, which is critical for further formulation of drug delivery systems into semisolid (gels, creams, lotions,

Pharmaceutics [GPAT] – Books [Study Notes] 7 in 1 Books with 2500+ Question Answer As Per Updated Syllabus

Pharmaceutics [GPAT] – Books [Study Notes] 7 in 1 Books with 2500+ Question Answer As Per Updated Syllabus
  • Author : DIWAKAR EDUCATION HUB
  • Publisher : DIWAKAR EDUCATION HUB
  • Release : 01 April 2022
GET THIS BOOKPharmaceutics [GPAT] – Books [Study Notes] 7 in 1 Books with 2500+ Question Answer As Per Updated Syllabus

Pharmaceutics [GPAT] – Books [Study Notes] 7 Books with 2500+ Question Answer As Per Updated Syllabus Design by Expert Faculties for Secure 152 Marks in Graduate Pharmacy Aptitude Test [ Asked 38 MCQ in Exam] Highlights of Books – As Per Updated Syllabus Graduate Pharmacy Aptitude Test 7 Booklets theory + MCQ In Each Book given 4 Chapters in Details [Total 28] Covered all 28 Chapters – Ex Pharmacy Profession & Introduction to Pharmaceuticals, Introduction to dosage form, Sources of drug information Total 2500 + Questions Answer [ Numerical with Explanation] Design by Pharma Professor & Topper Qualified

Proceedings of ICE-SEAM 2021: Special Edition

Proceedings of ICE-SEAM 2021: Special Edition
  • Author : Mohd Fadzli Bin Abdollah
  • Publisher : UTeM Press
  • Release : 01 April 2022
GET THIS BOOKProceedings of ICE-SEAM 2021: Special Edition

This e-book is a compilation of papers presented at the 7th International Conference and Exhibition on Sustainable Energy and Advanced Materials (ICE-SEAM 2021) - Virtual Platform, Malaysia on 23 November 2021. This special edition of proceedings has 17 selected papers that focus on IR4.0, including 3D printing and advanced materials, and how it might impact energy systems in numerous ways for sustainable development, especially during the pandemic COVID19.

Pharmaceutical Quality by Design

Pharmaceutical Quality by Design
  • Author : Sarwar Beg,Md Saquib Hasnain
  • Publisher : Academic Press
  • Release : 27 March 2019
GET THIS BOOKPharmaceutical Quality by Design

Pharmaceutical Quality by Design: Principles and Applications discusses the Quality by Design (QbD) concept implemented by regulatory agencies to ensure the development of a consistent and high-quality pharmaceutical product that safely provides the maximum therapeutic benefit to patients. The book walks readers through the QbD framework by covering the fundamental principles of QbD, the current regulatory requirements, and the applications of QbD at various stages of pharmaceutical product development, including drug substance and excipient development, analytical development, formulation development, dissolution

How to Design and Implement Powder-to-Tablet Continuous Manufacturing Systems

How to Design and Implement Powder-to-Tablet Continuous Manufacturing Systems
  • Author : Fernando Muzzio,Sarang Oka
  • Publisher : Elsevier
  • Release : 29 April 2022
GET THIS BOOKHow to Design and Implement Powder-to-Tablet Continuous Manufacturing Systems

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 operations, along with their characterization and control. In addition, it discusses practical insights and strategies that the editor and chapter authors have learned. Chapters cover Process Analytical Technology (PAT) tools and the application of PAT data to enable distributed process control.

Theory and Practice of Contemporary Pharmaceutics

Theory and Practice of Contemporary Pharmaceutics
  • Author : Tapash K. Ghosh,Bhaskara R. Jasti
  • Publisher : CRC Press
  • Release : 23 November 2004
GET THIS BOOKTheory and Practice of Contemporary Pharmaceutics

With a shift toward problem-based learning and critical thinking in many health science fields, professional pharmacy training faces a shift in focus as well. Although the Accreditation Council for Pharmacy Education (ACPE) has recently suggested guidelines for problem solving to be better integrated into pharmacy curriculum, pharmacy books currently available either address this material inadequately or lack it completely. Theory and Practice of Contemporary Pharmaceutics addresses this problem by challenging pharmacy students to think critically in preparation for situations that

Predictive Modeling of Pharmaceutical Unit Operations

Predictive Modeling of Pharmaceutical Unit Operations
  • Author : Preetanshu Pandey,Rahul Bharadwaj
  • Publisher : Woodhead Publishing
  • Release : 26 September 2016
GET THIS BOOKPredictive Modeling of Pharmaceutical Unit Operations

The use of modeling and simulation tools is rapidly gaining prominence in the pharmaceutical industry covering a wide range of applications. This book focuses on modeling and simulation tools as they pertain to drug product manufacturing processes, although similar principles and tools may apply to many other areas. Modeling tools can improve fundamental process understanding and provide valuable insights into the manufacturing processes, which can result in significant process improvements and cost savings. With FDA mandating the use of Quality

27th European Symposium on Computer Aided Process Engineering

27th European Symposium on Computer Aided Process Engineering
  • Author : Anonim
  • Publisher : Elsevier
  • Release : 21 September 2017
GET THIS BOOK27th European Symposium on Computer Aided Process Engineering

27th European Symposium on Computer Aided Process Engineering, Volume 40 contains the papers presented at the 27th European Society of Computer-Aided Process Engineering (ESCAPE) event held in Barcelona, October 1-5, 2017. It is a valuable resource for chemical engineers, chemical process engineers, researchers in industry and academia, students, and consultants for chemical industries. Presents findings and discussions from the 27th European Society of Computer-Aided Process Engineering (ESCAPE) event

How to Validate a Pharmaceutical Process

How to Validate a Pharmaceutical Process
  • Author : Steven Ostrove
  • Publisher : Academic Press
  • Release : 07 June 2016
GET THIS BOOKHow to Validate a Pharmaceutical Process

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 processes and protocols. It also addresses practical problems and offers solutions to qualify and validate a pharmaceutical process. Understanding the “why is critical to a successful and defensible process validation, making this book an essential research companion for all practitioners

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

Aulton's Pharmaceutics

Aulton's Pharmaceutics
  • Author : Michael E. Aulton,Kevin Taylor
  • Publisher : Elsevier Health Sciences
  • Release : 16 May 2022
GET THIS BOOKAulton's Pharmaceutics

Pharmaceutics is one of the most diverse subject areas in all of pharmaceutical science. In brief, it is concerned with the scientific and technological aspects of the design and manufacture of dosage forms or medicines. An understanding of pharmaceutics is therefore vital for all pharmacists and those pharmaceutical scientists who are involved with converting a drug or a potential drug into a medicine that can be delivered safely, effectively and conveniently to the patient. Now in its fourth edition, this

Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture

Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture
  • Author : Gintaras V. Reklaitis,Christine Seymour,Salvador García-Munoz
  • Publisher : John Wiley & Sons
  • Release : 01 September 2017
GET THIS BOOKComprehensive Quality by Design for Pharmaceutical Product Development and Manufacture

Covers a widespread view of Quality by Design (QbD) encompassing the many stages involved in the development of a new drug product. The book provides a broad view of Quality by Design (QbD) and shows how QbD concepts and analysis facilitate the development and manufacture of high quality products. QbD is seen as a framework for building process understanding, for implementing robust and effective manufacturing processes and provides the underpinnings for a science-based regulation of the pharmaceutical industry. Edited by