Download or read book Pharmacie gal nique CAMPUS written by Denis Brossard and published by Elsevier Health Sciences. This book was released on 2016-10-18 with total page 454 pages. Available in PDF, EPUB and Kindle. Book excerpt: La pharmacie galénique est non seulement l’art de préparer, conserver et présenter les nouveaux médicaments, mais aussi une science appliquée à prédominances tantôt technologiques (pharmacotechnie), tantôt biologiques (biodisponibilité). Cette 10e édition a été actualisée et enrichie en fonction des évolutions scientifiques, technologiques, et des apports récents des principaux référentiels de l’enseignement de la pharmacie galénique, à savoir : - Le Guide des bonnes pratiques de fabrication des médicaments de 2014. - Le Guide des bonnes pratiques de préparation de 2007. - La Pharmacopée européenne, 8e édition. - La Pharmacopée française, 11e édition révisée notamment pour le Formulaire National.
Download or read book Les bonnes pratiques de fabrication dans l industrie pharmaceutique written by Josée Bouchard and published by 2305, rue de l'Université. This book was released on 2009 with total page 313 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Canada Gazette written by Canada and published by . This book was released on 1997 with total page 1520 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book The Canada Gazette written by Canada and published by . This book was released on 1996 with total page 650 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Les bonnes pratiques de fabrication dans l industrie pharmaceutique written by Josée Bouchard (spécialiste en gestion de la qualité système).) and published by . This book was released on 2022 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Les bonnes pratiques de fabrication dans l industrie pharmaceutique written by Josée Bouchard (Spécialiste de la gestion) and published by . This book was released on 2022 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: "Édition courante qui comprend les exigences des bonnes pratiques de fabrication européennes (Eudralex et Agence nationale de sécurité du médicament et des produits de santé [ANSM]), canadiennes (Santé Canada) et américaines (Food and Drug Aministration [FDA]), incluant les récentes exigences liées à l’intégrité des données. Cet ouvrage reflète les courants modernes en gestion de la qualité en production pharmaceutique et les attentes des agences réglementaires concernant la fabrication, l’emballage, l’analyse, l’entreposage et la distribution des médicaments à usage humain ou vétérinaire. Il cerne les éléments essentiels à la production de médicaments de qualité. Ainsi, ce volume présente les connaissances de base et les principes fondamentaux de l’application des bonnes pratiques de fabrication durant la production manufacturière de produits thérapeutiques. Il permet de se familiariser avec les concepts afin de mieux interpréter l’essentiel des lignes directrices, en considérant les enjeux, les défis et les obstacles tant sur le plan de la conformité que sur celui de l’efficacité dans leur application. Des illustrations, des exemples et des exercices accompagnent le contenu de chaque chapitre."--Page 4 de la couverture
Download or read book Process Architecture in Biomanufacturing Facility Design written by Jeffery Odum and published by John Wiley & Sons. This book was released on 2018-01-26 with total page 381 pages. Available in PDF, EPUB and Kindle. Book excerpt: Essential information for architects, designers, engineers, equipment suppliers, and other professionals who are working in or entering the biopharmaceutical manufacturing field Biomanufacturing facilities that are designed and built today are radically different than in the past. The vital information and knowledge needed to design and construct these increasingly sophisticated biopharmaceutical manufacturing facilities is difficult to find in published literature—and it’s rarely taught in architecture or design schools. This is the first book for architects and designers that fills this void. Process Architecture in Biomanufacturing Facility Design provides information on design principles of biopharmaceutical manufacturing facilities that support emerging innovative processes and technologies, use state-of-the-art equipment, are energy efficient and sustainable, and meet regulatory requirements. Relying on their many years of hands-on design and operations experience, the authors emphasize concepts and practical approaches toward design, construction, and operation of biomanufacturing facilities, including product-process-facility relationships, closed systems and single use equipment, aseptic manufacturing considerations, design of biocontainment facility and process based laboratory, and sustainability considerations, as well as an outlook on the facility of the future. Provides guidelines for meeting licensing and regulatory requirements for biomanufacturing facilities in the U.S.A and WHO—especially in emerging global markets in India, China, Latin America, and the Asia/Pacific regions Focuses on innovative design and equipment, to speed construction and time to market, increase energy efficiency, and reduce footprint, construction and operational costs, as well as the financial risks associated with construction of a new facility prior to the approval of the manufactured products by regulatory agencies Includes many diagrams that clarify the design approach Process Architecture in Biomanufacturing Facility Design is an ideal text for professionals involved in the design of facilities for manufacturing of biopharmaceuticals and vaccines, biotechnology, and life-science industry, including architects and designers of industrial facilities, construction, equipment vendors, and mechanical engineers. It is also recommended for university instructors, advanced undergraduates, and graduate students in architecture, industrial engineering, mechanical engineering, industrial design, and industrial interior design.
Download or read book Single Use Technology in Biopharmaceutical Manufacture written by Regine Eibl and published by John Wiley & Sons. This book was released on 2019-07-18 with total page 367 pages. Available in PDF, EPUB and Kindle. Book excerpt: Authoritative guide to the principles, characteristics, engineering aspects, economics, and applications of disposables in the manufacture of biopharmaceuticals The revised and updated second edition of Single-Use Technology in Biopharmaceutical Manufacture offers a comprehensive examination of the most-commonly used disposables in the manufacture of biopharmaceuticals. The authors—noted experts on the topic—provide the essential information on the principles, characteristics, engineering aspects, economics, and applications. This authoritative guide contains the basic knowledge and information about disposable equipment. The author also discusses biopharmaceuticals’ applications through the lens of case studies that clearly illustrate the role of manufacturing, quality assurance, and environmental influences. This updated second edition revises existing information with recent developments that have taken place since the first edition was published. The book also presents the latest advances in the field of single-use technology and explores topics including applying single-use devices for microorganisms, human mesenchymal stem cells, and T-cells. This important book: • Contains an updated and end-to-end view of the development and manufacturing of single-use biologics • Helps in the identification of appropriate disposables and relevant vendors • Offers illustrative case studies that examine manufacturing, quality assurance, and environmental influences • Includes updated coverage on cross-functional/transversal dependencies, significant improvements made by suppliers, and the successful application of the single-use technologies Written for biopharmaceutical manufacturers, process developers, and biological and chemical engineers, Single-Use Technology in Biopharmaceutical Manufacture, 2nd Edition provides the information needed for professionals to come to an easier decision for or against disposable alternatives and to choose the appropriate system.
Download or read book Storyboarding written by Steven Price and published by Palgrave Macmillan. This book was released on 2015-10-08 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: This study provides the first book-length critical history of storyboarding, from the birth of cinema to the present day and beyond. It discusses the role of storyboarding in key films including Gone with the Wind , Psycho and The Empire Strikes Back , and is illustrated with a wide range of images.
Download or read book Pesticide Manual written by British Crop Protection Council and published by . This book was released on 1971 with total page 495 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Continuous Biomanufacturing written by Ganapathy Subramanian and published by John Wiley & Sons. This book was released on 2017-12-26 with total page 628 pages. Available in PDF, EPUB and Kindle. Book excerpt: This is the most comprehensive treatise of this topic available, providing invaluable information on the technological and economic benefits to be gained from implementing continuous processes in the biopharmaceutical industry. Top experts from industry and academia cover the latest technical developments in the field, describing the use of single-use technologies alongside perfusion production platforms and downstream operations. Special emphasis is given to process control and monitoring, including such topics as 'quality by design' and automation. The book is supplemented by case studies that highlight the enormous potential of continuous manufacturing for biopharmaceutical production facilities.
Download or read book Hepatocyte Transplantation written by Michio Mito and published by S. Karger AG (Switzerland). This book was released on 1997 with total page 372 pages. Available in PDF, EPUB and Kindle. Book excerpt: The rapidly increasing frequency of organ transplantation is causing a severe shortage of donor organs. Hepatocyte transplantation has thus been studied to develop an alternative therapeutic method for patients with various liver diseases. In experimental studies using rodents, transplanted hepatocytes survive and function in ectopic sites for a long period of time. Recent advances in molecular biology and tissue engineering enable us to manipulate isolated hepatocytes before transplantation. Before clinical application of this new therapeutic method, there are many issues to be resolved such as determining an optimal location for transplantation, rapid proliferation of transplanted hepatocytes, transplantation in large animals, immunological reactions and long-term gene expression. In this book, authorities on hepatocyte transplantation from all over the world describe progress in this field and discuss the unsolved problems. For researchers and clinicians interested in the liver, this book will be the definitive resource on hepatocyte transplantation.
Download or read book Making Medicines in Africa written by Maureen Mackintosh and published by Springer. This book was released on 2016-02-03 with total page 353 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book is open access under a CC-BY license. The importance of the pharmaceutical industry in Sub-Saharan Africa, its claim to policy priority, is rooted in the vast unmet health needs of the sub-continent. Making Medicines in Africa is a collective endeavour, by a group of contributors with a strong African and more broadly Southern presence, to find ways to link technological development, investment and industrial growth in pharmaceuticals to improve access to essential good quality medicines, as part of moving towards universal access to competent health care in Africa. The authors aim to shift the emphasis in international debate and initiatives towards sustained Africa-based and African-led initiatives to tackle this huge challenge. Without the technological, industrial, intellectual, organisational and research-related capabilities associated with competent pharmaceutical production, and without policies that pull the industrial sectors towards serving local health needs, the African sub-continent cannot generate the resources to tackle its populations' needs and demands. Research for this book has been selected as one of the 20 best examples of the impact of UK research on development. See http://www.ukcds.org.uk/the-global-impact-of-uk-research for further details.
Download or read book Pharmaceutical Isolators written by Brian Midcalf and published by Pharmaceutical Press. This book was released on 2004 with total page 292 pages. Available in PDF, EPUB and Kindle. Book excerpt: This work considers the basic concepts, definitions, and standards necessary in the design, construction, commissioning, maintenance, and use of pharmaceutical isolators.
Download or read book Alphaherpesviruses written by Sandra Knowles Weller and published by Caister Academic Press Limited. This book was released on 2011 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Alphaherpesviruses are a fascinating group of DNA viruses that includes important human pathogens such as herpes simplex virus type 1 (HSV-1), HSV-2, and varicella-zoster virus (VZV): the causative agents of cold sores, genital ulcerous disease, and chickenpox/shingles, respectively. A key attribute of these viruses is their ability to establish lifelong latent infection in the peripheral nervous system of the host. Such persistence requires subversion of the host's immune system and intrinsic antiviral defense mechanisms. Understanding the mechanisms of the immune evasion and what triggers viral reactivation is a major challenge for today's researchers. This has prompted enormous research efforts into understanding the molecular and cellular biology of these viruses. This up-to-date and comprehensive volume aims to distill the most important research in this area providing a timely overview of the field. Topics covered include: transcriptional regulation, DNA replication, translational control, virus entry and capsid assembly, the role of microRNAs in infection and oncolytic vectors for cancer therapy. In addition there is coverage of virus-host interactions, including apoptosis, subversion of host protein quality control and DNA damage response pathways, autophagy, establishment and reactivation from latency, interferon responses, immunity and vaccine development. Essential reading for everyone working with alphaherpesviruses and of interest to all virologists working on latent infections.
Download or read book International Scientific Affairs written by United States. Department of State. Office of Media Services and published by . This book was released on 1963 with total page 8 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book New and Nonofficial Remedies written by Council on Drugs (American Medical Association) and published by . This book was released on 1918 with total page 488 pages. Available in PDF, EPUB and Kindle. Book excerpt: Descriptions of therapeutic, prophylactic and diagnostic agents evaluated by the Council on Drugs.
