Enhancing Workflows in Biologics Drug Substance Process Development Through Automation

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Publisher :
ISBN 13 :
Total Pages : 0 pages
Book Rating : 4.:/5 (14 download)

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Book Synopsis Enhancing Workflows in Biologics Drug Substance Process Development Through Automation by : Alexander L. C. Judge

Download or read book Enhancing Workflows in Biologics Drug Substance Process Development Through Automation written by Alexander L. C. Judge and published by . This book was released on 2023 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: In the face of increasing competition, increasing pipeline complexity, and increasing resource requirements for bringing new drugs to market, streamlining process development is an important means of controlling costs and achieving competitive advantage in the biopharmaceutical industry. One potential means of achieving such improvements in process development is through the implementation of high throughput technologies, equipment (and associated methods and software) used to generate and process large amounts of data in little time. It is important, however, that implementation of these solutions is optimized across the entire process development organization rather than applications be deployed piecemeal within specific functions. This thesis develops a framework for identifying promising opportunities for use of high throughput technologies and quantifying the value that can be derived from their implementation. Though the framework is more broadly applicable than just to research and development organizations, the thesis is focused on its application to biologics process development within Amgen. It is used to assess the value of implementing a specific high throughput platform, Sartorius ambr® 250 systems, in upstream biologics process development. Through mapping and analyzing the workflows of Amgen's Biologics Drug Substance Technologies (Biologics DST) group, the implementation of this system was identified as a promising opportunity for employing high throughput technologies. In particular, a net present value (NPV) analysis was performed to show that investment in ambr 250 systems is likely to yield a positive NPV. However, the expected NPV depends strongly on both the expected useful lifetime of the systems and their capacity utilization. In addition, high throughput technologies provide substantial upside potential not captured in the NPV. Specifically, for the ambr 250 this includes cutting 6.5 weeks off development time for projects where process development is on the critical path. Using ambr 250 for Process Characterization (PC) on such programs could increase highly valuable weeks of sales. A framework was also developed for assessing how three models of staffing support for high throughput technologies affect the value that can be derived from their implementation. This framework was applied to the use of ambr 250 systems at Amgen to determine how to realize the maximum possible value from investment in this equipment. The assessment found that a dedicated team model is most likely to successfully facilitate the high capacity utilization and maximum potential useable life that are critical for achieving positive NPV. A formal subject matter expert (SME) model may also achieve these goals at lower cost, though at higher risk. The informal champion model, however, is advised against. The recommended path forward is to purchase one or two ambr systems to use in Commercial Process Development (CPD) and to establish whether they can be used for PC. Once it is established that the ambr 250 can be used for PC, it is recommended that the existing systems be used immediately thereafter on key projects for which increased development speed can increase speed to market, and that a third system be purchased to expand capacity. Though this work focuses specifically on process development at Amgen, the frameworks developed herein are broadly applicable to many types of organizations, from R&D to manufacturing to the service sector. In any industry where high throughput technologies exist, these frameworks can be used to identify promising opportunities for their implementation, quantify the value they can provide to determine if investment is worthwhile, and decide how they should be supported to maximize the value realized by the organization.

Accelerating Process Development for Biologics on an Automated, Pharmacy-scale Manufacturing System

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Publisher :
ISBN 13 :
Total Pages : 197 pages
Book Rating : 4.:/5 (119 download)

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Book Synopsis Accelerating Process Development for Biologics on an Automated, Pharmacy-scale Manufacturing System by : Laura Ellen Crowell

Download or read book Accelerating Process Development for Biologics on an Automated, Pharmacy-scale Manufacturing System written by Laura Ellen Crowell and published by . This book was released on 2020 with total page 197 pages. Available in PDF, EPUB and Kindle. Book excerpt: The conventional large-scale, centralized, single-product manufacturing model for biologic drugs does not allow for the economical production of drugs for small patient populations or for the distribution of these drugs in developing countries. A decentralized model featuring small-scale, fully automated, multi-product manufacturing of biologics at the point-of-care could address some of these issues. To truly realize the benefits of such a manufacturing paradigm, it must also be paired with rapid process development methods for the production of new molecules. In this thesis, we describe the development of a bench-scale, automated, multi-product manufacturing system for the end-to-end production of hundreds to thousands of doses of clinical quality protein medicines in about three days. We then demonstrate the application of this platform to the manufacture of a trivalent vaccine in a single campaign through co-expression and co-purification. We further demonstrate new methodologies for the accelerated development of manufacturing processes to produce new molecules on the system including a strategy for the development and optimization of fully integrated, multi-column processes for straight-through chromatographic purification, and the development of a platform process for the production and purification of single-domain antibodies. We then propose a workflow for the collection of a dataset relating the chromatographic behavior of host-cell proteins to their biophysical characteristics with the goal of building an in silico tool for the prediction of purification processes for any new molecule. Finally, we propose a platform approach, as opposed to a platform process, for the development of manufacturing processes for new biologics which is based on gaining a deeper understanding of process development challenges with regard to the host and to the molecule itself. Ultimately, we believe that the combination of a small-scale, automated manufacturing platform and accelerated strategies for developing processes to manufacture new products on the platform could enable time- and cost-efficient manufacturing of a wide variety of biologic drugs, increasing access to medicines throughout the world.

PAT Applied in Biopharmaceutical Process Development And Manufacturing

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Publisher : CRC Press
ISBN 13 : 1439829454
Total Pages : 330 pages
Book Rating : 4.4/5 (398 download)

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Book Synopsis PAT Applied in Biopharmaceutical Process Development And Manufacturing by : Cenk Undey

Download or read book PAT Applied in Biopharmaceutical Process Development And Manufacturing written by Cenk Undey and published by CRC Press. This book was released on 2011-12-07 with total page 330 pages. Available in PDF, EPUB and Kindle. Book excerpt: As with all of pharmaceutical production, the regulatory environment for the production of therapeutics has been changing as a direct result of the US FDA-initiated Quality by Design (QbD) guidelines and corresponding activities of the International Committee for Harmonization (ICH). Given the rapid growth in the biopharmaceutical area and the complexity of the molecules, the optimum use of which are still being developed, there is a great need for flexible and proactive teams in order to satisfy the regulatory requirements during process development. Process Analytical Technologies (PAT) applied in biopharmaceutical process development and manufacturing have received significant attention in recent years as an enabler to the QbD paradigm. PAT Applied in Biopharmaceutical Process Development and Manufacturing covers technological advances in measurement sciences, data acquisition, monitoring, and control. Technical leaders present real-life case studies in areas including measuring and monitoring raw materials, cell culture, purification, and cleaning and lyophilization processes via advanced PAT. They also explore how data are collected and analyzed using advanced analytical techniques such as multivariate data analysis, monitoring, and control in real-time. Invaluable for experienced practitioners in PAT in biopharmaceuticals, this book is an excellent reference guide for regulatory officials and a vital training aid for students who need to learn the state of the art in this interdisciplinary and exciting area.

Automation Applications in Bio-pharmaceuticals

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Publisher : ISA
ISBN 13 : 9781934394250
Total Pages : 324 pages
Book Rating : 4.3/5 (942 download)

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Book Synopsis Automation Applications in Bio-pharmaceuticals by : George Buckbee (P.E.)

Download or read book Automation Applications in Bio-pharmaceuticals written by George Buckbee (P.E.) and published by ISA. This book was released on 2008 with total page 324 pages. Available in PDF, EPUB and Kindle. Book excerpt: A guide for engineers and designers new to the field of bio-pharmaceutical process control. For the experienced automation professional, it outlines the unique design and application issues for the bio-pharmaceutical industry. For those already familiar with this industry, it provides specific advice for automating these processes.

Quality by Design for Biopharmaceutical Drug Product Development

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Publisher : Springer
ISBN 13 : 1493923161
Total Pages : 710 pages
Book Rating : 4.4/5 (939 download)

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Book Synopsis Quality by Design for Biopharmaceutical Drug Product Development by : Feroz Jameel

Download or read book Quality by Design for Biopharmaceutical Drug Product Development written by Feroz Jameel and published by Springer. This book was released on 2015-04-01 with total page 710 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume explores the application of Quality by Design (QbD) to biopharmaceutical drug product development. Twenty-eight comprehensive chapters cover dosage forms, liquid and lyophilized drug products. The introductory chapters of this book define key elements of QbD and examine how these elements are integrated into drug product development. These chapters also discuss lessons learned from the FDA Office of Biotechnology Products pilot program. Following chapters demonstrate how QbD is used for formulation development ranging from screening of formulations to developability assessment to development of lyophilized and liquid formats. The next few chapters study the use of small-scale and surrogate models as well as QbD application to drug product processes such as drug substance freezing and thawing, mixing, sterile filtration, filling, lyophilization, inspection and shipping and handling. Later chapters describe more specialized applications of QbD in the drug product realm. This includes the use of QbD in primary containers, devices and combination product development. The volume also explores QbD applied to vaccine development, automation, mathematical modeling and monitoring, and controlling processes and defining control strategies. It concludes with a discussion on the application of QbD to drug product technology transfer as well as overall regulatory considerations and lifecycle management. Quality by Design for Biopharmaceutical Drug Product Development is an authoritative resource for scientists and researchers interested in expanding their knowledge on QbD principles and uses in creating better drugs.

Continuous Manufacturing for the Modernization of Pharmaceutical Production

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Publisher : National Academies Press
ISBN 13 : 0309487811
Total Pages : 69 pages
Book Rating : 4.3/5 (94 download)

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Book Synopsis Continuous Manufacturing for the Modernization of Pharmaceutical Production by : National Academies of Sciences, Engineering, and Medicine

Download or read book Continuous Manufacturing for the Modernization of Pharmaceutical Production written by National Academies of Sciences, Engineering, and Medicine and published by National Academies Press. This book was released on 2019-04-05 with total page 69 pages. Available in PDF, EPUB and Kindle. Book excerpt: On July 30-31, 2018, the National Academies of Sciences, Engineering, and Medicine held a workshop titled Continuous Manufacturing for the Modernization of Pharmaceutical Production. This workshop discussed the business and regulatory concerns associated with adopting continuous manufacturing techniques to produce biologics such as enzymes, monoclonal antibodies, and vaccines. The participants also discussed specific challenges for integration across the manufacturing system, including upstream and downstream processes, analytical techniques, and drug product development. The workshop addressed these challenges broadly across the biologics domain but focused particularly on drug categories of greatest FDA and industrial interest such as monoclonal antibodies and vaccines. This publication summarizes the presentations and discussions from the workshop.

Artificial Intelligence in Drug Discovery

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Publisher : Royal Society of Chemistry
ISBN 13 : 1839160543
Total Pages : 425 pages
Book Rating : 4.8/5 (391 download)

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Book Synopsis Artificial Intelligence in Drug Discovery by : Nathan Brown

Download or read book Artificial Intelligence in Drug Discovery written by Nathan Brown and published by Royal Society of Chemistry. This book was released on 2020-11-04 with total page 425 pages. Available in PDF, EPUB and Kindle. Book excerpt: Following significant advances in deep learning and related areas interest in artificial intelligence (AI) has rapidly grown. In particular, the application of AI in drug discovery provides an opportunity to tackle challenges that previously have been difficult to solve, such as predicting properties, designing molecules and optimising synthetic routes. Artificial Intelligence in Drug Discovery aims to introduce the reader to AI and machine learning tools and techniques, and to outline specific challenges including designing new molecular structures, synthesis planning and simulation. Providing a wealth of information from leading experts in the field this book is ideal for students, postgraduates and established researchers in both industry and academia.

Guideline on General Principles of Process Validation

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Publisher :
ISBN 13 :
Total Pages : 32 pages
Book Rating : 4.3/5 (91 download)

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Book Synopsis Guideline on General Principles of Process Validation by :

Download or read book Guideline on General Principles of Process Validation written by and published by . This book was released on 1987 with total page 32 pages. Available in PDF, EPUB and Kindle. Book excerpt:

TEXTBOOK OF COMPUTER AIDED DRUG DEVELOPMENT

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Publisher : Shashwat Publication
ISBN 13 : 9360874108
Total Pages : 316 pages
Book Rating : 4.3/5 (68 download)

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Book Synopsis TEXTBOOK OF COMPUTER AIDED DRUG DEVELOPMENT by : Dr. Surya Devarakonda, Dr. Purma Aravinda Reddy , Dr. Divya Yada , Ms. Bansi H. Zalavadia , Dr. Reeta Sethi

Download or read book TEXTBOOK OF COMPUTER AIDED DRUG DEVELOPMENT written by Dr. Surya Devarakonda, Dr. Purma Aravinda Reddy , Dr. Divya Yada , Ms. Bansi H. Zalavadia , Dr. Reeta Sethi and published by Shashwat Publication. This book was released on 2024-09-02 with total page 316 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book explores the use of computer-assisted techniques in the discovery, design, optimization, and production of innovative pharmaceutical formulations and drug delivery systems, with an emphasis on their effectiveness and safety. It discusses computational methods, statistical and molecular modeling, all aimed at advancing the development and safe administration of drugs in humans. The book thoroughly examines the integration of Quality by Design (QbD), Design of Experiments (DoE), artificial intelligence, and in silico pharmacokinetic assessment/simulation, facilitated by commercial software and expert systems, and includes examples from recent research. "Computer-aided Pharmaceutics and Drug Delivery" serves as a comprehensive reference for the latest scholarly updates on emerging developments in computer-assisted techniques for drug design and development. It is intended for pharmacists, medical practitioners, students, and researchers seeking authoritative insights into this evolving field.

Continuous Manufacturing of Pharmaceuticals

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Publisher : John Wiley & Sons
ISBN 13 : 1119001323
Total Pages : 645 pages
Book Rating : 4.1/5 (19 download)

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Book Synopsis Continuous Manufacturing of Pharmaceuticals by : Peter Kleinebudde

Download or read book Continuous Manufacturing of Pharmaceuticals written by Peter Kleinebudde and published by John Wiley & Sons. This book was released on 2017-09-05 with total page 645 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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 on a continuous basis; and enhanced process reliability and flexibility. Continuous Manufacturing of Pharmaceuticals prepares professionals to take advantage of that exciting new approach to improving drug manufacturing efficiency. This book covers key aspects of the continuous manufacturing of pharmaceuticals. The first part provides an overview of key chemical engineering principles and the current regulatory environment. The second covers existing technologies for manufacturing both small-molecule-based products and protein/peptide products. The following section is devoted to process analytical tools for continuously operating manufacturing environments. The final two sections treat the integration of several individual parts of processing into fully operating continuous process systems and summarize state-of-art approaches for innovative new manufacturing principles. Brings together the essential know-how for anyone working in drug manufacturing, as well as chemical, food, and pharmaceutical scientists working on continuous processing Covers chemical engineering principles, regulatory aspects, primary and secondary manufacturing, process analytical technology and quality-by-design Contains contributions from researchers in leading pharmaceutical companies, the FDA, and academic institutions Offers an extremely well-informed look at the most promising future approaches to continuous manufacturing of innovative pharmaceutical products Timely, comprehensive, and authoritative, Continuous Manufacturing of Pharmaceuticals is an important professional resource for researchers in industry and academe working in the fields of pharmaceuticals development and manufacturing.

Current Developments in Biotechnology and Bioengineering

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Publisher : Elsevier
ISBN 13 : 0444636749
Total Pages : 852 pages
Book Rating : 4.4/5 (446 download)

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Book Synopsis Current Developments in Biotechnology and Bioengineering by : Christian Larroche

Download or read book Current Developments in Biotechnology and Bioengineering written by Christian Larroche and published by Elsevier. This book was released on 2016-09-17 with total page 852 pages. Available in PDF, EPUB and Kindle. Book excerpt: Current Developments in Biotechnology and Bioengineering: Bioprocesses, Bioreactors and Controls provides extensive coverage of new developments, state-of-the-art technologies, and potential future trends, reviewing industrial biotechnology and bioengineering practices that facilitate and enhance the transition of processes from lab to plant scale, which is becoming increasingly important as such transitions continue to grow in frequency. Focusing on industrial bioprocesses, bioreactors for bioprocesses, and controls for bioprocesses, this title reviews industrial practice to identify bottlenecks and propose solutions, highlighting that the optimal control of a bioprocess involves not only maximization of product yield, but also taking into account parameters such as quality assurance and environmental aspects. Describes industrial bioprocesses based on the reaction media Lists the type of bioreactors used for a specific bioprocess/application Outlines the principles of control systems in various bioprocesses

Semantic Web: Concepts, Technologies and Applications

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Publisher : Springer Science & Business Media
ISBN 13 : 184628581X
Total Pages : 329 pages
Book Rating : 4.8/5 (462 download)

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Book Synopsis Semantic Web: Concepts, Technologies and Applications by : Karin Breitman

Download or read book Semantic Web: Concepts, Technologies and Applications written by Karin Breitman and published by Springer Science & Business Media. This book was released on 2007-01-24 with total page 329 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Web is growing at an astounding pace surpassing the 8 billion page mark. However, most pages are still designed for human consumption and cannot be processed by machines. This book provides a well-paced introduction to the Semantic Web. It covers a wide range of topics, from new trends (ontologies, rules) to existing technologies (Web Services and software agents) to more formal aspects (logic and inference). It includes: real-world (and complete) examples of the application of Semantic Web concepts; how the technology presented and discussed throughout the book can be extended to other application areas.

Ex Vivo Cell Therapy

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Publisher : Academic Press
ISBN 13 :
Total Pages : 392 pages
Book Rating : 4.3/5 (91 download)

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Book Synopsis Ex Vivo Cell Therapy by : Klaus Schindhelm

Download or read book Ex Vivo Cell Therapy written by Klaus Schindhelm and published by Academic Press. This book was released on 1999 with total page 392 pages. Available in PDF, EPUB and Kindle. Book excerpt: R.E. Nordon and K. Schindhelm, Introduction. -- L. Robb, A.G. Elefanty, and C.G. Begley, Transcriptional Control of Hematopoieses. -- R. Starr and N.A. Nicola, Cell Signaling by Hemopoietic Growth Factor Receptors. -- P.J. Simmons, D.N. Haylock, and J.-P. Lévesque, Influence of Cytokines and Adhesion Molecules on Hematopoietic Stem Cell Development. -- P.A. Rowlings, Allogeneic Hematopoietic Stem Cell Transplantation. -- U. Hahn and L.B. To, Autologous Stem Cell Transplantation. -- M.R. Vowels, Cord Blood Stem Cell Transplantation. -- S.R. Riddell, E.H. Warren, D. Lewinsohn, C. Yee, and P.D. Greenberg, Reconstitution of Immunity by Adoptive Immunotherapy with T Cells. -- L.Q. Sun, M. Miller, and G. Symonds, Exogenous Gene Transfer into Lymphoid and Hematopoietic Progenitor Cells. -- C. Dowding, T. Leemhuis, A. Jakubowski, and C. Reading, Process Development for Ex Vivo Cell Therapy. -- R.E. Nordon and K. Schindhelm, Cell Separation. -- P.W. Zandstra, C.J. Eaves, and J.M. Piret, Environ ...

Continuous Processing in Pharmaceutical Manufacturing

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Publisher : John Wiley & Sons
ISBN 13 : 3527335951
Total Pages : 528 pages
Book Rating : 4.5/5 (273 download)

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Book Synopsis Continuous Processing in Pharmaceutical Manufacturing by : Ganapathy Subramanian

Download or read book Continuous Processing in Pharmaceutical Manufacturing written by Ganapathy Subramanian and published by John Wiley & Sons. This book was released on 2015-02-09 with total page 528 pages. Available in PDF, EPUB and Kindle. Book excerpt: With contributions from biotechnologists and bioengineers, this ready reference describes the state of the art in industrial biopharmaceutical production, with a strong focus on continuous processes. Recent advances in single-use technology as well as application guidelines for all types of biopharmaceutical products, from vaccines to antibodies, and from bacterial to insect to mammalian cells are covered. The efficiency, robustness, and quality control of continuous production processes for biopharmaceuticals are reviewed and compared to traditional batch processes for a range of different production systems.

Chemical Engineering in the Pharmaceutical Industry, Active Pharmaceutical Ingredients

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Publisher : John Wiley & Sons
ISBN 13 : 1119285887
Total Pages : 1168 pages
Book Rating : 4.1/5 (192 download)

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Book Synopsis Chemical Engineering in the Pharmaceutical Industry, Active Pharmaceutical Ingredients by : David J. am Ende

Download or read book Chemical Engineering in the Pharmaceutical Industry, Active Pharmaceutical Ingredients written by David J. am Ende and published by John Wiley & Sons. This book was released on 2019-03-28 with total page 1168 pages. Available in PDF, EPUB and Kindle. Book excerpt: A guide to the development and manufacturing of pharmaceutical products written for professionals in the industry, revised second edition The revised and updated second edition of Chemical Engineering in the Pharmaceutical Industry is a practical book that highlights chemistry and chemical engineering. The book’s regulatory quality strategies target the development and manufacturing of pharmaceutically active ingredients of pharmaceutical products. The expanded second edition contains revised content with many new case studies and additional example calculations that are of interest to chemical engineers. The 2nd Edition is divided into two separate books: 1) Active Pharmaceutical Ingredients (API’s) and 2) Drug Product Design, Development and Modeling. The active pharmaceutical ingredients book puts the focus on the chemistry, chemical engineering, and unit operations specific to development and manufacturing of the active ingredients of the pharmaceutical product. The drug substance operations section includes information on chemical reactions, mixing, distillations, extractions, crystallizations, filtration, drying, and wet and dry milling. In addition, the book includes many applications of process modeling and modern software tools that are geared toward batch-scale and continuous drug substance pharmaceutical operations. This updated second edition: • Contains 30new chapters or revised chapters specific to API, covering topics including: manufacturing quality by design, computational approaches, continuous manufacturing, crystallization and final form, process safety • Expanded topics of scale-up, continuous processing, applications of thermodynamics and thermodynamic modeling, filtration and drying • Presents updated and expanded example calculations • Includes contributions from noted experts in the field Written for pharmaceutical engineers, chemical engineers, undergraduate and graduate students, and professionals in the field of pharmaceutical sciences and manufacturing, the second edition of Chemical Engineering in the Pharmaceutical Industry focuses on the development and chemical engineering as well as operations specific to the design, formulation, and manufacture of drug substance and products.

Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture

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Publisher : John Wiley & Sons
ISBN 13 : 0470942371
Total Pages : 418 pages
Book Rating : 4.4/5 (79 download)

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Book Synopsis Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture by : Gintaras V. Reklaitis

Download or read book Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture written by Gintaras V. Reklaitis and published by John Wiley & Sons. This book was released on 2017-10-09 with total page 418 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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 the three renowned researchers in the field, Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture guides pharmaceutical engineers and scientists involved in product and process development, as well as teachers, on how to utilize QbD practices and applications effectively while complying with government regulations. The material is divided into three main sections: the first six chapters address the role of key technologies, including process modeling, process analytical technology, automated process control and statistical methodology in supporting QbD and establishing the associated design space. The second section consisting of seven chapters present a range of thoroughly developed case studies in which the tools and methodologies discussed in the first section are used to support specific drug substance and drug-product QbD related developments. The last section discussed the needs for integrated tools and reviews the status of information technology tools available for systematic data and knowledge management to support QbD and related activities. Highlights Demonstrates Quality by Design (QbD) concepts through concrete detailed industrial case studies involving of the use of best practices and assessment of regulatory implications Chapters are devoted to applications of QbD methodology in three main processing sectors—drug substance process development, oral drug product manufacture, parenteral product processing, and solid-liquid processing Reviews the spectrum of process model types and their relevance, the range of state-of-the-art real-time monitoring tools and chemometrics, and alternative automatic process control strategies and methods for both batch and continuous processes The role of the design space is demonstrated through specific examples and the importance of understanding the risk management aspects of design space definition is highlighted Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture is an ideal book for practitioners, researchers, and graduate students involved in the development, research, or studying of a new drug and its associated manufacturing process.

3D Printing of Pharmaceuticals and Drug Delivery Devices

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Publisher : MDPI
ISBN 13 : 3039364235
Total Pages : 436 pages
Book Rating : 4.0/5 (393 download)

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Book Synopsis 3D Printing of Pharmaceuticals and Drug Delivery Devices by : Dimitrios A. Lamprou

Download or read book 3D Printing of Pharmaceuticals and Drug Delivery Devices written by Dimitrios A. Lamprou and published by MDPI. This book was released on 2020-07-01 with total page 436 pages. Available in PDF, EPUB and Kindle. Book excerpt: The 3D printing (3DP) process was patented in 1986; however, only in the last decade has it begun to be used for medical applications, as well as in the fields of prosthetics, bio-fabrication, and pharmaceutical printing. 3DP or additive manufacturing (AM) is a family of technologies that implement layer-by-layer processes in order to fabricate physical models based on a computer aided design (CAD) model. 3D printing permits the fabrication of high degrees of complexity with great reproducibility in a fast and cost-effective fashion. 3DP technology offers a new paradigm for the direct manufacture of individual dosage forms and has the potential to allow for variations in size and geometry as well as control dose and release behavior. Furthermore, the low cost and ease of use of 3DP systems means that the possibility of manufacturing medicines and medical devices at the point of dispensing or at the point of use could become a reality. 3DP thus offers the perfect innovative manufacturing route to address the critical capability gap that hinders the widespread exploitation of personalized medicines for molecules that are currently not easy to deliver. This Special Issue will address new developments in the area of 3D printing and bioprinting for drug delivery applications, covering the recent advantages and future directions of additive manufacturing for pharmaceutical products.