Formulation Development And Manufacturing Of Vaccines

Exam Prep For Formulation Development And Manufacturing Of  Book PDF
✏Book Title : Exam Prep for Formulation Development and Manufacturing of
✏Author :
✏Publisher :
✏Release Date :
✏Pages :
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Exam Prep for Formulation Development and Manufacturing of Book Summary :

Vaccine Development And Manufacturing Book PDF
✏Book Title : Vaccine Development and Manufacturing
✏Author : Emily P. Wen
✏Publisher : John Wiley & Sons
✏Release Date : 2014-10-06
✏Pages : 456
✏ISBN : 9781118870907
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Vaccine Development and Manufacturing Book Summary : Vaccine Manufacturing and Production is an invaluable reference on how to produce a vaccine - from beginning to end - addressing all classes of vaccines from a processing, production, and regulatory viewpoint. It will provide comprehensive information on the various fields involved in the production of vaccines, from fermentation, purification, formulation, to regulatory filing and facility designs. In recent years, there have been tremendous advances in all aspects of vaccine manufacturing. Improved technology and growth media have been developed for the production of cell culture with high cell density or fermentation. Vaccine Manufacturing and Production will serve as a reference on all aspects of vaccine production by providing an in-depth description of the available technologies for making different types of vaccines and the current thinking in facility designs and supply issues. This book will provide insight to the issues scientists face when producing a vaccine, the steps that are involved, and will serve as a reference tool regarding state-of-the-art vaccine manufacturing technologies and facility set-up. Highlights include: Comprehensive coverage of vaccine production : from a process point of view- fermentation to purification to formulation developments; from a production point of view - from facility design to manufacturing; and from a regulatory point of view - requirements from government agencies Authors from different major pharmaceutical and biotechnology companies Describes the challenges and issues involved in vaccine production and manufacturing of the different classes of vaccines, an area not covered by other books currently on the market

Lyophilized Biologics And Vaccines Book PDF
✏Book Title : Lyophilized Biologics and Vaccines
✏Author : Dushyant Varshney
✏Publisher : Springer
✏Release Date : 2015-05-19
✏Pages : 401
✏ISBN : 9781493923830
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Lyophilized Biologics and Vaccines Book Summary : This book provides a detailed account of the most recent developments, challenges and solutions to seamlessly advance and launch a lyophilized biologics or vaccine product, based on diverse modalities, ranging from antibodies (e.g., monoclonal, fused), complex biologics (e.g., antibody drug conjugate, PEGylated proteins), and vaccines (e.g., recombinant-protein based). The authors adeptly guide the reader through all crucial aspects, from biophysical and chemical stability considerations of proteins, analytical methods, advances in controlled ice nucleation and quality-by-design approaches, alternate drying technology, to latest regulatory, packaging and technology transfer considerations to develop a stable, safe and effective therapeutic protein, vaccine and biotechnology products. Lyophilized Biologics and Vaccines: Modality-Based Approaches is composed of four sections with a total of 17 chapters. It serves as a reference to all critical assessments and steps from early pre-formulation stages to product launch: Provides recent understanding of heterogeneity of protein environment and selection of appropriate buffer for stabilization of lyophilized formulations Details the latest developments in instrumental analysis and controlled ice nucleation technology Explains in-depth lyophilized (or dehydrated) formulation strategies considering diverse modalities of biologics and vaccines, including plasmid DNA and lipid-based therapeutics Details an exhaustive update on quality-by-design and process analytical technology approaches, illustrated superbly by case studies and FDA perspective Provides the latest detailed account of alternate drying technologies including spray drying, bulk freeze-drying and crystallization, supported exceptionally by case studies Provides a step-by-step guide through critical considerations during process scale-up, technology transfer, packaging and drug delivery device selection, for a successful lyophilization process validation, regulatory submission and product launch Chapters are written by one or more world-renowned leading authorities from academia, industry or regulatory agencies, whose expertise cover lyophilization of the diverse modalities of biopharmaceuticals. Their contributions are based on the exhaustive review of literature coupled with excellent hands-on experiences in laboratory or GMP setup, making this an exceptional guide to all stages of lyophilized or dehydrated product development.

Practical Aspects Of Vaccine Development Book PDF
✏Book Title : Practical Aspects of Vaccine Development
✏Author : Satoshi Ohtake
✏Publisher : Academic Press
✏Release Date : 2020-12-01
✏Pages : 410
✏ISBN : 9780128143582
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Practical Aspects of Vaccine Development Book Summary : Practical Aspects of Vaccine Development provides an academic and industry perspective on vaccine development and manufacturing. With the increasing complexity of vaccine products in development, there is a need for a comprehensive review of the current state of the industry and challenges being encountered. While formulation scientists working in biotherapeutic development may be familiar with proteins, vaccines present unique challenges. Vaccines include a wide range of components including proteins, polysaccharides, protein-polysaccharide conjugates, adjuvants, and more. The container closure system may also be unique, and the product may require freezing storage or lyophilization based on the stability of the vaccine components. Based on the route of delivery, novel technologies and devices may be required. Covering formulation development, manufacture, and delivery considerations of vaccine production, this book is essential to formulation scientists, researchers in vaccine development throughout medical and life sciences, and advanced students. Includes formulation considerations for various vaccine types, including proteins, polysaccharides, conjugates, and live vaccines Covers process development for solution, suspension, and lyophilized products Explores the future of vaccines, including multi-component vaccines and novel delivery mechanisms/devices

Biological Drug Products Book PDF
✏Book Title : Biological Drug Products
✏Author : Wei Wang
✏Publisher : John Wiley & Sons
✏Release Date : 2013-08-29
✏Pages : 744
✏ISBN : 9781118695227
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Biological Drug Products Book Summary : Tested and proven solutions to the challenges of biologicaldrug product development Biological drug products play a central role in combating humandiseases; however, developing new successful biological drugspresents many challenges, including labor intensive productionprocesses, tighter regulatory controls, and increased marketcompetition. This book reviews the current state of the science,offering readers a single resource that sets forth the fundamentalsas well as tested and proven development strategies for biologicaldrugs. Moreover, the book prepares readers for the challenges thattypically arise during drug development, offering straightforwardsolutions to improve their ability to pass through all theregulatory hurdles and deliver new drug products to the market. Biological Drug Products begins with generalconsiderations for the development of any biological drug productand then explores the strategies and challenges involved in thedevelopment of specific types of biologics. Divided into fiveparts, the book examines: Part 1: General Aspects Part 2: Proteins and Peptides Part 3: Vaccines Part 4: Novel Biologics Part 5: Product Administration/Delivery Each chapter has been prepared by one or more leading experts inbiological drug development. Contributions are based on acomprehensive review and analysis of the current literature as wellas the authors' first-hand experience developing and testing newdrugs. References at the end of each chapter serve as a gateway tooriginal research papers and reviews in the field. By incorporating lessons learned and future directions forresearch, Biological Drug Products enables pharmaceuticalscientists and students to improve their success rate in developingnew biologics to treat a broad range of human diseases.

Parenteral Medications Fourth Edition Book PDF
✏Book Title : Parenteral Medications Fourth Edition
✏Author : Sandeep Nema
✏Publisher : CRC Press
✏Release Date : 2019-08-08
✏Pages : 1125
✏ISBN : 9780429574726
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Parenteral Medications Fourth Edition Book Summary : Parenteral Medications is an authoritative, comprehensive reference work on the formulation and manufacturing of parenteral dosage forms, effectively balancing theoretical considerations with practical aspects of their development. Previously published as a three-volume set, all volumes have been combined into one comprehensive publication that addresses the plethora of changes in the science and considerable advances in the technology associated with these products and routes of administration. Key Features: Provides a comprehensive reference work on the formulation and manufacturing of parenteral dosage forms Addresses changes in the science and advances in the technology associated with parenteral medications and routes of administration Includes 13 new chapters and updated chapters throughout Contains the contributors of leading researchers in the field of parenteral medications Uses full color detailed illustrations, enhancing the learning process The fourth edition not only reflects enhanced content in all the chapters but also highlights the rapidly advancing formulation, processing, manufacturing parenteral technology including advanced delivery and cell therapies. The book is divided into seven sectionss: Section 1 - Parenteral Drug Administration and Delivery Devices; Section 2 - Formulation Design and Development; Section 3 - Specialized Drug Delivery Systems; Section 4 - Primary Packaging and Container Closure Integrity; Section 5 - Facility Design and Environmental Control; Section 6 - Sterilization and Pharmaceutical Processing; Section 7 - Quality Testing and Regulatory Requirements

📒Vaccinology ✍ Gregg N. Milligan

Vaccinology Book PDF
✏Book Title : Vaccinology
✏Author : Gregg N. Milligan
✏Publisher : John Wiley & Sons
✏Release Date : 2014-12-04
✏Pages : 400
✏ISBN : 9781118636527
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Vaccinology Book Summary : Vaccinology: An Essential Guide outlines in a clear,practical format the entire vaccine development process, fromconceptualization and basic immunological principles through toclinical testing and licensing of vaccines. With anoutstanding introduction to the history and practice ofvaccinology, it also guides the reader through the basic sciencerelating to host immune responses to pathogens. Covering the safety, regulatory, ethical, and economicand geographical issues that drive vaccine development and trials,it also presents vaccine delivery strategies, novel vaccineplatforms (including experimental vaccines and pathogens), antigendevelopment and selection, vaccine modelling, and the developmentof vaccines against emerging pathogens and agents of bioterror.There are also sections devoted to veterinary vaccines andassociated regulatory processes. Vaccinology: An Essential Guide is a perfect tool fordesigned for undergraduate and graduate microbiologists andimmunologists, as well as residents, fellows and trainees ofinfectious disease and vaccinology. It is also suitable for allthose involved in designing and conducting clinical vaccine trials,and is the ideal companion to the larger reference bookVaccinology: Principles and Practice.

Continuous Processing In Pharmaceutical Manufacturing Book PDF
✏Book Title : Continuous Processing in Pharmaceutical Manufacturing
✏Author : Ganapathy Subramanian
✏Publisher : John Wiley & Sons
✏Release Date : 2014-12-03
✏Pages : 528
✏ISBN : 9783527673704
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Continuous Processing in Pharmaceutical Manufacturing Book Summary : 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.

📒Vaccines ✍ Stanley A. Plotkin

Vaccines Book PDF
✏Book Title : Vaccines
✏Author : Stanley A. Plotkin
✏Publisher : Elsevier Health Sciences
✏Release Date : 2008
✏Pages : 1725
✏ISBN : 9781416036111
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Vaccines Book Summary : Completely revised and updated, this respected reference offers comprehensive and current coverage of every aspect of vaccination--from development to use in reducing disease. It also includes access to a companion Web site for more coverage.

The Role Of The Study Director In Nonclinical Studies Book PDF
✏Book Title : The Role of the Study Director in Nonclinical Studies
✏Author : William J. Brock
✏Publisher : John Wiley & Sons
✏Release Date : 2014-05-02
✏Pages : 560
✏ISBN : 9781118874080
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏The Role of the Study Director in Nonclinical Studies Book Summary : A single-source reference with a broad and holistic overview of nonclinical studies, this book offers critical training material and describes regulations of nonclinical testing through guidelines, models, case studies, practical examples, and worldwide perspectives. The book: Provides a complete overview of nonclinical study organization, conduct, and reporting and describes the roles and responsibilities of a Study Director to manage an effective study Covers regulatory and scientific concepts, including international testing and Good Laboratory Practice (GLP), compliance with guidelines, and animal models Features a concluding chapter that compiles case studies / lessons learned from those that have served as a Study Director for many years Addresses the entire spectrum of nonclinical testing, making it applicable to those in the government, laboratories and those actively involved in in all sectors of industry

📒Development Of Novel Vaccines ✍ Alexander von Gabain

Development Of Novel Vaccines Book PDF
✏Book Title : Development of Novel Vaccines
✏Author : Alexander von Gabain
✏Publisher : Springer Science & Business Media
✏Release Date : 2012-04-23
✏Pages : 306
✏ISBN : 9783709107096
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Development of Novel Vaccines Book Summary : “Development of novel vaccines” gives an overview of the tasks in basic research leading to the final product – the vaccine and its applications, belonging to the most complex biologics in the pharmaceutical field. Distinct from most textbooks in the vaccine arena, the current issue focuses on the translational aspect, namely, how research results can be transformed into life-saving medical interventions. Each chapter of the book deals with one important paradigm for the development of novel vaccines, along the value chain towards the final vaccine, and furthermore, with the inevitable tools required for this process. Contributions are prepared by teams of scientists, all of whom are experts in the field, most of them anchored in biomedical organizations devoted to translational culture, thereby lighting the certain topics from different views. This volume is a must read for researchers engaged in vaccine development and who really want to see their research results to become a product.

Influenza Vaccine Federal Investments In Alternative Technologies And Challenges To Development And Licensure Book PDF
✏Book Title : Influenza Vaccine Federal Investments in Alternative Technologies and Challenges to Development and Licensure
✏Author : Marcia Crosse
✏Publisher : DIANE Publishing
✏Release Date : 2011-10-07
✏Pages : 58
✏ISBN : 9781437988291
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Influenza Vaccine Federal Investments in Alternative Technologies and Challenges to Development and Licensure Book Summary : Production delays for the 2009 H1N1 pandemic vaccine using the current egg-based production technology heightened interest in alternative technologies that could expand the supply or accelerate the availability of influenza vaccine. Within the federal government, the Dept. of Health and Human Services (HHS) and the Dept. of Defense (DOD) support the development of technologies that can be used in producing technologies that can be used in producing influenza vaccines. HHS's Food and Drug Admin. (FDA) reviews licensing applications for new vaccine, and the Dept. of State is the U.S. diplomatic liaison to the international entity that declares worldwide pandemics. This report examines (1) federal funding from FY 2005 through March 2011 for alternative technologies and the status of manufacturers' efforts, (2) challenges to development and licensure identified by stakeholders, and (3) how HHS is addressing those challenges. Tables and figures. This is a print on demand report.

Novel Technologies For Vaccine Development Book PDF
✏Book Title : Novel Technologies for Vaccine Development
✏Author : Igor S Lukashevich
✏Publisher : Springer
✏Release Date : 2014-11-13
✏Pages : 386
✏ISBN : 9783709118184
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Novel Technologies for Vaccine Development Book Summary : This book presents a detailed overview of the development of new viral vector-based vaccines before discussing two major applications: preventive vaccines for infectious diseases and therapeutic cancer vaccines. Viral vector-based vaccines hold a great potential for development into successful pharmaceutical products and several examples at the advanced pre-clinical or clinical stage are presented. Nevertheless, the most efforts were focused on novel and very innovative technologies for new generation of vector-based vaccines. Furthermore, specific topics such as delivery and adjuvant and protection strategies for cell-mediated-based vaccines are presented. Given its scope, the book is a “must read” for all those involved in vaccine development, both in academia and industrial vaccine development.

📒Mucosal Vaccines ✍ Pamela A. Kozlowski

Mucosal Vaccines Book PDF
✏Book Title : Mucosal Vaccines
✏Author : Pamela A. Kozlowski
✏Publisher : Springer Science & Business Media
✏Release Date : 2012-01-13
✏Pages : 198
✏ISBN : 9783642236921
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Mucosal Vaccines Book Summary : This volume is focused on the development of vaccines which generate immune effectors capable of blocking mucosal entry or peripheral pathogen spread. A critical first step in the design of mucosal vaccines is the selection of administration route. Not all mucosal immunization routes are created equally when it comes to eliciting immune responses in multiple body compartments. This subject and situations when a mucosal route may not be required for vaccine delivery are reviewed here with an emphasis on the sublingual immunization route, which may offer a safer alternative to the nasal route for induction of broadly disseminated immune responses. External host defenses that inhibit entry of microorganisms at mucosal surfaces also pose obstacles to the efficient internalization of mucosally-applied vaccines. Transcutaneous immunization with appropriate adjuvants and permeation enhancers can induce mucosal immune responses and may be advantageous for bypassing these luminal barriers. Other chapters describe strategies for enhancing uptake of mucosal vaccines, for instance through targeted delivery to antigen-sampling M cells, construction of virus-like particles which mimic natural pathogens, addition of mucoadhesives or formulation as nanoparticles. Topics include edible vaccines as well as plant-based production of subunit or particulate vaccines that could be administered by any route. Dry powder vaccines that could be insufflated or directly applied to mucosal surfaces may be particularly ideal for mass vaccination in developing countries. The manufacture, stability and efficacy of powder formulations is comprehensively reviewed. We conclude with chapters on two of the greatest challenges facing mucosal vaccine development: human immunodeficiency virus and bioterrorist agents. This monograph highlights progress and information that should prove invaluable for the development of contemporary vaccines that prevent infection by these and other mucosal pathogens.

Formulation And Process Development Strategies For Manufacturing Biopharmaceuticals Book PDF
✏Book Title : Formulation and Process Development Strategies for Manufacturing Biopharmaceuticals
✏Author : Feroz Jameel
✏Publisher : John Wiley & Sons
✏Release Date : 2010-08-09
✏Pages : 984
✏ISBN : 9780470118122
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Formulation and Process Development Strategies for Manufacturing Biopharmaceuticals Book Summary : A real-world guide to the production and manufacturing of biopharmaceuticals While much has been written about the science of biopharmaceuticals, there is a need for practical, up-to-date information on key issues at all stages of developing and manufacturing commercially viable biopharmaceutical drug products. This book helps fill the gap in the field, examining all areas of biopharmaceuticals manufacturing, from development and formulation to production and packaging. Written by a group of experts from industry and academia, the book focuses on real-world methods for maintaining product integrity throughout the commercialization process, clearly explaining the fundamentals and essential pathways for all development stages. Coverage includes: Research and early development phase–appropriate approaches for ensuring product stability Development of commercially viable formulations for liquid and lyophilized dosage forms Optimal storage, packaging, and shipping methods Case studies relating to therapeutic monoclonal antibodies, recombinant proteins, and plasma fractions Useful analysis of successful and failed products Formulation and Process Development Strategies for Manufacturing Biopharma-ceuticals is an essential resource for scientists and engineers in the pharmaceutical and biotech industries, for government and regulatory agencies, and for anyone with an interest in the latest developments in the field.

Sterile Product Development Book PDF
✏Book Title : Sterile Product Development
✏Author : Parag Kolhe
✏Publisher : Springer Science & Business Media
✏Release Date : 2013-10-12
✏Pages : 585
✏ISBN : 9781461479789
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Sterile Product Development Book Summary : This comprehensive book encompasses various facets of sterile product development. Key concepts relevant to the successful development of sterile products are illustrated through case studies and are covered under three sections in this book: • Formulation approaches that discuss a variety of dosage forms including protein therapeutics, lipid-based controlled delivery systems, PEGylated biotherapeutics, nasal dosage form, and vaccines • Process, container closure and delivery considerations including freeze-thaw process challenges, best practices for technology transfer to enable commercial product development, innovations and advancement in aseptic fill-finish operations, approaches to manufacturing lyophilized parenteral products, pen / auto-injector delivery devices, and associated container closure integrity testing hurdles for sterile product closures • Regulatory and quality aspects in the areas of particulate matter and appearance evaluation, sterile filtration, admixture compatibility considerations, sterilization process considerations, microbial contamination investigations and validation of rapid microbiological methods, and dry and moist heat sterilizers This book is a useful resource to scientists and researchers in both industry and academia, and it gives process and product development engineers insight into current industry practices and evolving regulatory expectations for sterile product development.

Vaccine Analysis Strategies Principles And Control Book PDF
✏Book Title : Vaccine Analysis Strategies Principles and Control
✏Author : Brian K. Nunnally
✏Publisher : Springer
✏Release Date : 2014-11-27
✏Pages : 665
✏ISBN : 9783662450246
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Vaccine Analysis Strategies Principles and Control Book Summary : This book is an indispensable tool for anyone involved in the research, development, or manufacture of new or existing vaccines. It describes a wide array of analytical and quality control technologies for the diverse vaccine modalities. Topics covered include the application of both classical and modern bio-analytical tools; procedures to assure safety and control of cross contamination; consistent biological transition of vaccines from the research laboratory to manufacturing scale; whole infectious attenuated organisms, such as live-attenuated and inactivated whole-cell bacterial vaccines and antiviral vaccines using attenuated or inactivated viruses; principles of viral inactivation and the application of these principles to vaccine development; recombinant DNA approaches to produce modern prophylactic vaccines; bacterial subunit, polysaccharide and glycoconjugate vaccines; combination vaccines that contain multiple antigens as well as regulatory requirements and the hurdles of licensure.

Combined Vaccines And Simultaneous Administration Book PDF
✏Book Title : Combined Vaccines and Simultaneous Administration
✏Author : Jim C. Williams
✏Publisher :
✏Release Date : 1995
✏Pages : 404
✏ISBN : UVA:X002240592
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Combined Vaccines and Simultaneous Administration Book Summary : This text brings together contributions from members of the scientific, public health and regulatory communities on areas of vaccinology addressing safety, immunogenicity, protective efficacy, development of immunologic correlates of protection and manufacturing issues. Scientific advances and regulatory issues bearing on the development of combination vaccines and vaccines for simultaneous administration are discussed. The goals and impact of the Children's Vaccines Initiative are considered.

📒Science ✍ John Michels (Journalist)

Science Book PDF
✏Book Title : Science
✏Author : John Michels (Journalist)
✏Publisher :
✏Release Date : 2006
✏Pages :
✏ISBN : MINN:31951P00977730A
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Science Book Summary :

Immunomic Discovery Of Adjuvants And Candidate Subunit Vaccines Book PDF
✏Book Title : Immunomic Discovery of Adjuvants and Candidate Subunit Vaccines
✏Author : Darren R. Flower
✏Publisher : Springer Science & Business Media
✏Release Date : 2012-12-09
✏Pages : 314
✏ISBN : 9781461450702
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Immunomic Discovery of Adjuvants and Candidate Subunit Vaccines Book Summary : This volume will address an important emergent area within the field of immunomics: the discovery of antigens and adjuvants within the context of reverse vaccinology. Conventional approaches to vaccine design and development requires pathogens to be cultivated in the laboratory and the immunogenic molecules within them to be identifiable. Conventional vaccinology is no longer universally successful, particularly for recalcitrant pathogens. By using genomic information we can study vaccine development in silico: 'reverse vaccinology', can identify candidate subunits vaccines by identifying antigenic proteins and by using equally rational approaches to identify novel immune response-enhancing adjuvants.

Drugs Advances In Research And Application 2011 Edition Book PDF
✏Book Title : Drugs Advances in Research and Application 2011 Edition
✏Author :
✏Publisher : ScholarlyEditions
✏Release Date : 2012-01-09
✏Pages : 891
✏ISBN : 9781464920929
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Drugs Advances in Research and Application 2011 Edition Book Summary : Drugs: Advances in Research and Application: 2011 Edition is a ScholarlyEditions™ eBook that delivers timely, authoritative, and comprehensive information about Trials. The editors have built Drugs: Advances in Research and Application: 2011 Edition on the vast information databases of ScholarlyNews.™ You can expect the information about Trials in this eBook to be deeper than what you can access anywhere else, as well as consistently reliable, authoritative, informed, and relevant. The content of Drugs: Advances in Research and Application: 2011 Edition has been produced by the world’s leading scientists, engineers, analysts, research institutions, and companies. All of the content is from peer-reviewed sources, and all of it is written, assembled, and edited by the editors at ScholarlyEditions™ and available exclusively from us. You now have a source you can cite with authority, confidence, and credibility. More information is available at

The Role Of Diaspora In Technology Transfer And Achieving Sustainable Development In Sudan Book PDF
✏Book Title : The Role of Diaspora in Technology Transfer and Achieving Sustainable Development in Sudan
✏Author : Allam Ahmed
✏Publisher : Routledge
✏Release Date : 2009
✏Pages : 214
✏ISBN : UOM:39015080880043
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏The Role of Diaspora in Technology Transfer and Achieving Sustainable Development in Sudan Book Summary : This volume includes a wide range (research areas and topics) of papers, projects, proposals and case studies presented during the First Sudanese Diaspora International Conference, held in January 2009 in Brighton, United Kingdom.Sudan like much of the rest of the developing world has toyed with and abided by various approaches or strategies to transfer technology (TT) and achieve sustainable development (SD) without reaping any significant socio-economic benefits. The Sudanese diasporic community is relatively large and has a significant impact on Sudan development on account of the size and volume of financial remittances. However diasporic contribution is largely neglected within national science and technology policies and strategies. Adopting a more holistic approach, the conference aims to provide a stimulus for knowledge exchange and discussion that focuses on issues relating to the role of diaspora in TT and achieving SD to critically examine the relations and links between diaspora, Sudan and host countries, and attempts to outline policy and strategies to support the role of diaspora in developing, creating wealth and achieving SD in Sudan. The conference also aims to learn lessons from the successful communities across the world and emulate the ideas and innovations of these communities by Sudan.It is hoped that the ensemble of papers presented in this volume will help to stimulate debate amongst scholars, researchers and policymakers and that readers will find this volume interesting and thought-provoking. The seven main sections include: Diaspora Contribution to Home CountryTechnology and Scientific Knowledge TransferEducation, Training and DevelopmentMedical Sciences and Public HealthEngineering Applications and Sustainable Business ExcellenceEnvironment and Waste ManagementAbstracts for Oral Presentations

📒Fish Vaccination ✍ Roar Gudding

Fish Vaccination Book PDF
✏Book Title : Fish Vaccination
✏Author : Roar Gudding
✏Publisher : John Wiley & Sons
✏Release Date : 2014-03-04
✏Pages : 408
✏ISBN : 9781118806937
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Fish Vaccination Book Summary : Fish farming, in seawater and in freshwater, in cages, tanks or ponds, makes an ever-increasing and significant contribution to the production of aquatic food in many regions of the world. During the last few decades there has been significant progress and expansion in the aquaculture sector, characterized by intensified production and the exploitation of many new species. Aquaculture must be a sustainable bio-production, environmentally as well as economically. Disease prevention in order to reduce losses, and the use of antimicrobials is crucial in this perspective. Vaccination has, in a few years, become the most important method for disease prevention in aquaculture, and effective prophylaxis based on stimulation of the immune system of the fish is essential for further development of the industry. This book provides general information about disease prevention in fish by vaccination, as well as specific descriptions of the correct use of vaccines against the most important bacterial and viral infectious diseases of aquatic animals. The book is written by some of the world’s leading experts in the subject, drawn from many countries where aquaculture is a significant and expanding part of the economy. Fish Vaccination is an encyclopedia of fish vaccinology for every present and future aquaculturist. Professionals in the aquaculture sector, including fish veterinarians and fish biologists, within the industry, in scientific institutions and regulatory authorities will all find a huge wealth of commercially important knowledge within this book. Libraries in all universities where aquaculture, biological and veterinary sciences are studied and taught should have copies of this important book on their shelves.

📒Vaccine Protocols ✍ Andrew Robinson

Vaccine Protocols Book PDF
✏Book Title : Vaccine Protocols
✏Author : Andrew Robinson
✏Publisher : Springer Science & Business Media
✏Release Date : 2003
✏Pages : 414
✏ISBN : 9781592593996
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Vaccine Protocols Book Summary : This extensively revised, updated, and expanded second edition of a classic laboratory manual applies new understanding of molecular mechanisms to the rational design and development of vaccines. Here the working researcher will find readily reproducible techniques for the development and production of live attenuated vaccines, and vaccines based on inactivated toxins, peptides, and polysaccharide conjugates.

Formulation Tools For Pharmaceutical Development Book PDF
✏Book Title : Formulation tools for Pharmaceutical Development
✏Author : J E Aguilar
✏Publisher : Elsevier
✏Release Date : 2013-09-30
✏Pages : 304
✏ISBN : 9781908818508
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Formulation tools for Pharmaceutical Development Book Summary : A range of new and innovative tools used for preformulation and formulation of medicines help optimize pharmaceutical development projects. Such tools also assist with the performance evaluation of the pharmaceutical process, allowing any potential gaps to be identified. These tools can be applied in both basic research and industrial environment. Formulation tools for pharmaceutical development considers these key research and industrial tools. Nine chapters by leading contributors cover: Artificial neural networks technology to model, understand, and optimize drug formulations; ME_expert 2.0: a heuristic decision support system for microemulsions formulation development; Expert system for the development and formulation of push-pull osmotic pump tablets containing poorly water-soluble drugs; SeDeM Diagram: an expert system for preformulation, characterization and optimization of tables obtained by direct compression; New SeDeM-ODT expert system: an expert system for formulation of orodispersible tablets obtained by direct compression; and 3D-cellular automata in computer-aided design of pharmaceutical formulations: mathematical concept and F-CAD software. Coverage of artificial intelligence tools, new expert systems, understanding of pharmaceutical processes, robust development of medicines, and new ways to develop medicines Development of drugs and medicines using mathematical tools Compilation of expert system developed around the world

Encyclopedia Of Medical Organizations And Agencies Book PDF
✏Book Title : Encyclopedia of Medical Organizations and Agencies
✏Author : Gale Group
✏Publisher : Gale Cengage
✏Release Date : 2004-08-01
✏Pages : 1953
✏ISBN : 0787669008
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Encyclopedia of Medical Organizations and Agencies Book Summary : pThis resource brings you instant access to public and private agencies concerned with medical information, funding, research, education, planning, advocacy, advice and service. pSixty-nine subject chapters represent an entire range of contemporary medical fields: allergy and immunology, alternative medicine, biomedicine, chiropractic, gastroenterology, hypnosis, neurology, osteopathic medicine, reproduction and family planning, substance abuse and more. Entries provide contact and descriptive information for the organizations listed. A name and keyword index, as well as a subject cross-index, make finding information easy.

Therapeutic Protein Drug Products Book PDF
✏Book Title : Therapeutic Protein Drug Products
✏Author : Brian K Meyer
✏Publisher : Elsevier
✏Release Date : 2012-01-02
✏Pages : 200
✏ISBN : 9781908818102
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Therapeutic Protein Drug Products Book Summary : Therapeutic protein drug products provides a comprehensive overview of therapeutic protein drug products, with an emphasis on formulation beginning in the laboratory, followed by manufacturing and administration in the clinic. A list of many commercial therapeutic drug products are described and include the product name, dosages, active concentration, buffer, excipients, Ph, container type and route of administration. The laboratory formulation sections focus on the most common buffers, excipients, and Ph ranges that are commonly tested in addition to systematic approaches. A brief section on biophysical and analytical analysis is also provided. Properties of therapeutic protein formulations are described and include opalescence, phase separation, color, and subvisible particles. An emphasis is placed on material and process testing to ensure success during manufacturing. The drug product manufacturing process, which includes the process of compounding to filling, is also covered. Methods of delivery in the clinic are addressed, as well as delivery strategies. Finally, a perspective on the regulatory requirements for therapeutic protein formulations is discussed. Provides a list and description of commercially available therapeutic drug products and their formulations A comprehensive and practical overview of protein formulation in the laboratory, manufacturing, and the clinic Discusses recent topics including high protein concentration, phase separation, opalescence, and subvisible particles

📒Vaccine Adjuvants ✍ Derek T. O'Hagan

Vaccine Adjuvants Book PDF
✏Book Title : Vaccine Adjuvants
✏Author : Derek T. O'Hagan
✏Publisher : Springer Science & Business Media
✏Release Date : 2000
✏Pages : 354
✏ISBN : 9781592590834
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Vaccine Adjuvants Book Summary : Annotation Derek T. O'Hagan and a team of expert vaccinologists and pharmacologists thoroughly describe the preparation, characterization, and evaluation of a wide range of alternative vaccine adjuvants for use in preclinical studies. Each chapter carefully reviews a single adjuvant, and suggests why a specific adjuvant might be preferred for a given antigen, depending on what type of immune response is desired. Alternate adjuvant choices are also presented so that researchers can choose those most efficacious for their specific purpose. Comprehensive and highly practical, Vaccine Adjuvants: Preparation Methods and Research Protocols provides an effective guide to making and using vaccine adjuvants. By closely following directions from the book, today's researchers will be able optimally to induce specific immune responses against different types of antigens and to selectively manipulate the immune response in a favorable way.

📒Biomedical Engineering Handbook 2 ✍ Joseph D. Bronzino

Biomedical Engineering Handbook 2 Book PDF
✏Book Title : Biomedical Engineering Handbook 2
✏Author : Joseph D. Bronzino
✏Publisher : Springer Science & Business Media
✏Release Date : 2000-02-15
✏Pages :
✏ISBN : 354066808X
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Biomedical Engineering Handbook 2 Book Summary :

Government Research Directory Book PDF
✏Book Title : Government Research Directory
✏Author : Anonimo
✏Publisher : Gale Cengage
✏Release Date : 2008
✏Pages : 1485
✏ISBN : 0787697567
✏Available Language : English, Spanish, And French

Click Here To Get Book

✏Government Research Directory Book Summary : Provides more than 6,800 research facilities and programs of the U.S. and Canadian federal governments. Listings include e-mail and Web site addresses, and a wealth of descriptive information.