Download or read book Ma trise de la qualit fournisseurs et sous traitants au sein d un tablissement pharmaceutique written by Pauline Garnier and published by . This book was released on 2012 with total page 284 pages. Available in PDF, EPUB and Kindle. Book excerpt: Cette thèse a pour but de décrire la maîtrise de la qualité fournisseurs et sous-traitants dans l’industrie pharmaceutique. En effet, ce processus est long et complexe et demande ainsi d’être parfaitement compris et connu pour en assurer un déroulement optimal. Sa complexité s’explique par le nombre important d’acteurs et par la relation de partenariat qui doit s’établir entre le fournisseur/sous-traitants et le client, dans le but d’obtenir la meilleur Qualité possible du produit. Cet ouvrage décrit toutes les étapes suivies pour maîtriser cette Qualité, de l’expression du besoin, en passant par l’agrément et l’audit Qualité externe, jusqu’au suivi du fournisseur/sous-traitant. La notion d’amélioration continue est également traitée puisqu’elle doit s’appliquer à tous les niveaux du processus. Pour finir, cette thèse s’inscrit dans le cadre d’un stage effectué au Laboratoire français du Fractionnement et des Biotechnologies, dans le service Assurance Qualité Fournisseur. Cet ouvrage présente, l’analyse du processus propre au LFB, par rapport, aux différentes normes en vigueur.

Download or read book La ma trise des fournisseurs chez un fa onnier de l industrie pharmaceutique written by Jennifer Regnard and published by . This book was released on 2015 with total page 152 pages. Available in PDF, EPUB and Kindle. Book excerpt: La not ion de l a Qualité a évolué au cours du temps et notamment au sein d e l 'industrie pharmaceutique. Cette notion a d'abord été assimilée à un contrôle. Concernant la maîtri se des composants fou rnis, autrefois les matières premières uti lisées dans la fabrication de médicaments ne faisaient q ue l 'objet d'un contrôle à réception par les laboratoires pharmaceutiques. Ce seul contrôle a montré ses limites (on ne trouve que ce quel 'on cherche) et l a mise sous assurance qualité des fournisseurs s'est révélée nécessa ire. La maîtrise des fournisseurs est a lors apparue afin de garantir la qualité des matières utilisées dans la fabrication de méd icaments et donc de garantir la qualité finale du produit fini et la sécurité du patient. Pour ce faire,l 'ensemble des fournisseurs doit être qualifié. Différents critères sont requis pour cette qualification: audit sur si te chez le fourni sseur ou bien a u d it documentaire (questionnaire), contrat qualité et évaluation périodique satisfa isante du fournisseur. Une délégati on de contrôle/prélèvement peut être m ise en place avec un fournisseur. Dans ce cas, l 'évaluation de son système qualité est plus exigeante et il est dit certifié. Cette thèse traite de la démarche de mise sous Assurance Qualité de l 'ensemble des fournisseurs à maîtriser sur un site de production pharmaceutique : matières premières, artic les de conditionnement, sous-traitants, prestataires de services et consommables ainsi que des problématiques rencontrées chez un façonnier.

Download or read book La ma trise de l ensemble des fournisseurs d un site de production pharmaceutique written by Marie Yriarte and published by . This book was released on 2014 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: L'industrie pharmaceutique met en place un système qualité performant pour pouvoir maîtriser l'ensemble de ses fournisseurs. La maîtrise des fournisseurs permet d'assurer la qualité finale du produit pharmaceutique et de garantir la sécurité du patient. Des référentiels internationaux, européens et nationaux vont permettre la mise en place de ce processus de maîtrise des fournisseurs. En fonction du type de fournisseur, l'industrie pharmaceutique doit respecter les exigences de certains référentiels obligatoires ou a le choix du référentiel à appliquer pour maîtriser ses fournisseurs. Le processus de maitrise des fournisseurs comprend plusieurs étapes : la sélection, l'approbation, le suivi et la gestion des fournisseurs. L'industrie pharmaceutique peut établir un partenariat avec certains fournisseurs. Ce partenariat permet à l'industrie pharmaceutique de se concentrer sur son cœur de métier en délégant des contrôles ou des prélèvements aux fournisseurs. L'application de ce processus chez un sous-traitant pharmaceutique est également traitée dans cet ouvrage.

Download or read book Relation client fournisseur written by Sophie Belingheri and published by . This book was released on 2011 with total page 298 pages. Available in PDF, EPUB and Kindle. Book excerpt: L’instauration d’une Relation Client-Fournisseur (RCF) permettant de coopérer, de partager les ressources et de saisir les opportunités d’amélioration, tant avec les donneurs d’ordre qu’avec les différents fournisseurs, est un atout majeur pour perdurer et se développer dans un environnement aussi instable et concurrentiel que celui de la sous-traitance de fabrication pour l’Industrie pharmaceutique. L’objet de cette thèse est de décrire la construction d’une Relation Client-Fournisseur entre un sous-traitant de fabrication et ses fournisseurs de matières premières (MP) et d’articles de conditionnement (AdC) à travers la mise en place d’un système de maitrise qualité des fournisseurs. Ce système de maitrise qualité des fournisseurs s’articule autour de trois sous-processus interdépendants : l’agrément des couples fournisseur/fourniture, l’évaluation de la performance des couples fournisseur/fourniture agréés et la gestion des réclamations fournisseur.

Download or read book Ma trise qualit des partenaires externes d une entreprise pharmaceutique commerciale written by Tom Di Domizio and published by . This book was released on 2023 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Doing Business 2020 written by World Bank and published by World Bank Publications. This book was released on 2019-11-21 with total page 241 pages. Available in PDF, EPUB and Kindle. Book excerpt: Seventeen in a series of annual reports comparing business regulation in 190 economies, Doing Business 2020 measures aspects of regulation affecting 10 areas of everyday business activity.

Download or read book Supply Chain Management written by John T. Mentzer and published by SAGE. This book was released on 2001 with total page 530 pages. Available in PDF, EPUB and Kindle. Book excerpt: This work presents a comprehensive model of supply chain management. Experienced executives from 20 companies clearly define supply chain management, identifying those factors that contribute to its effective implementation. They provide practical guidelines on how companies can manage supply chains, addressing the role of all the traditional business functions in supply chain management and suggest how the adoption of a supply chain management approach can affect business strategy and corporate performance.

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 368 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 Global Burden of Disease and Risk Factors written by Alan D. Lopez and published by World Bank Publications. This book was released on 2006-04-02 with total page 511 pages. Available in PDF, EPUB and Kindle. Book excerpt: Strategic health planning, the cornerstone of initiatives designed to achieve health improvement goals around the world, requires an understanding of the comparative burden of diseases and injuries, their corresponding risk factors and the likely effects of invervention options. The Global Burden of Disease framework, originally published in 1990, has been widely adopted as the preferred method for health accounting and has become the standard to guide the setting of health research priorities. This publication sets out an updated assessment of the situation, with an analysis of trends observed since 1990 and a chapter on the sensitivity of GBD estimates to various sources of uncertainty in methods and data.

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 2nd Pan African Symposium on the Sustainable Use of Natural Resources in Africa written by Bihini won wa Musiti and published by IUCN. This book was released on 2003 with total page 344 pages. Available in PDF, EPUB and Kindle. Book excerpt: This bilingual publication results from a four-day symposium aimed at capturing the general directions and analytical issues that characterize approaches to sustainable use in Africa. The papers included in this work are organized under four major headings: modes of use, devolution, scale issues and external issues. Authors explore these themes through the use of case studies and the description of specific regional experiences. External issues are further explored in a series of commissioned policy papers which have also been included.

Download or read book Integrity in Public Procurement Good Practice from A to Z written by OECD and published by OECD Publishing. This book was released on 2007-05-31 with total page 180 pages. Available in PDF, EPUB and Kindle. Book excerpt: Provides, for the first time, a comparative overview of practices from A to Z. It maps out practices to enhance integrity throughout the whole procurement cycle, from needs assessment to contract management. It also takes a global stance by including practices from non-OECD countries.

Download or read book Frontline and Factory written by Roy MacLeod and published by Springer Science & Business Media. This book was released on 2007-05-06 with total page 292 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book represents a first considered attempt to study the factors that conditioned industrial chemistry for war in 1914-18. Taking a comparative perspective, it reflects on the experience of France, Germany, Austria, Russia, Britain, Italy and Russia, and points to significant similarities and differences. It looks at changing patterns in the organisation of industry, and at the emerging symbiosis between science, industry and the military.

Download or read book Faecal Sludge Management written by Linda Strande and published by IWA Publishing. This book was released on 2014-08-15 with total page 428 pages. Available in PDF, EPUB and Kindle. Book excerpt: It is estimated that literally billions of residents in urban and peri-urban areas of Africa, Asia, and Latin America are served by onsite sanitation systems (e.g. various types of latrines and septic tanks). Until recently, the management of faecal sludge from these onsite systems has been grossly neglected, partially as a result of them being considered temporary solutions until sewer-based systems could be implemented. However, the perception of onsite or decentralized sanitation technologies for urban areas is gradually changing, and is increasingly being considered as long-term, sustainable options in urban areas, especially in low- and middle-income countries that lack sewer infrastructures. This is the first book dedicated to faecal sludge management. It compiles the current state of knowledge of the rapidly evolving field of faecal sludge management, and presents an integrated approach that includes technology, management, and planning based on Sandecs 20 years of experience in the field. Faecal Sludge Management: Systems Approach for Implementation and Operation addresses the organization of the entire faecal sludge management service chain, from the collection and transport of sludge, and the current state of knowledge of treatment options, to the final end use or disposal of treated sludge. The book also presents important factors to consider when evaluating and upscaling new treatment technology options. The book is designed for undergraduate and graduate students, and engineers and practitioners in the field who have some basic knowledge of environmental and/or wastewater engineering.

Download or read book Oxford Textbook of Palliative Medicine written by Nathan I. Cherny and published by Oxford University Press, USA. This book was released on 2015 with total page 1281 pages. Available in PDF, EPUB and Kindle. Book excerpt: Emphasising the multi-disciplinary nature of palliative care the fourth edition of this text also looks at the individual professional roles that contribute to the best-quality palliative care.

Download or read book Oxford Textbook of Palliative Care for Children written by Richard Hain and published by Oxford University Press. This book was released on 2021-03-24 with total page 535 pages. Available in PDF, EPUB and Kindle. Book excerpt: The importance of palliative care for children facing life threatening illness and their families is now widely acknowledged as an essential part of care, which should be available to all children and families, throughout the child's illness and at the end of life. The new edition of the Oxford Textbook of Palliative Care for Children brings together the most up to date information, current knowledge, evidence, and developments of clinical practice in the field. The book is structured into four sections. 'Foundations of Care' describes core issues, the foundations on which paediatric palliative care is based. 'Child and Family Care' looks at different aspects of psychological, social, and cultural care for the sick child or young person, and their family. These chapters cover the time course of the illness, around the time of death and support for the bereaved family. 'Symptom Care' focuses on the uses of medication, specific symptoms, and their management. Finally, 'Delivery of Care' examines practical approaches to care in different environments and the needs of clinicians. Two new editors join the team from Canada and South Africa, reflecting our aims to contribute towards the development of care for children across the world, and to be a resource for both experienced clinicians and those new to the field. Comprehensive in scope, exhaustive in detail, and definitive in authority, this third edition has been thoroughly updated to cover new practices, current epidemiological data, and the evolving models that support the delivery of palliative medicine to children. This includes two new chapters, looking in detail at 'Decision Making' and 'Perinatal Care', and a new section highlighting the emerging importance of 'Palliative Care for Children in Humanitarian Crises'. This book is an essential resource for anyone who works with children worldwide.

Download or read book The Life Cycle of Pharmaceuticals in the Environment written by B.M. Peake and published by Elsevier. This book was released on 2015-11-13 with total page 272 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Life-Cycle of Pharmaceuticals in the Environment identifies pathways of entry of pharmaceuticals into the environment, beginning with the role of global prescribing and disposal practices. The book then discusses typical levels of common pharmaceuticals and how they can be determined in natural waters such as raw and treated sewage, and in potable water. In addition, sections examine methods currently available to degrade pharmaceuticals in natural waters and some of their ecotoxicological impacts, along with future considerations and the growing concept of product stewardship. Encompasses the full lifecycle of common pharmaceuticals, from prescription and dispensing practices to their occurrence in a range of different types of natural waters and their environmental impact Explores the role of the healthcare system and its affect on users Beneficial for environmental engineers involved in the design and operation of appropriate degradation technologies of the pharmaceutical prescription and disposal practices