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Supply Chain Management In The Drug Industry

Author: Hedley Rees
Publisher: John Wiley & Sons
ISBN: 0470922842
Size: 69.23 MB
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This book bridges the gap between practitioners of supply-chain management and pharmaceutical industry experts. It aims to help both these groups understand the different worlds they live in and how to jointly contribute to meaningful improvements in supply-chains within the globally important pharmaceutical sector. Scientific and technical staff must work closely with supply-chain practitioners and other relevant parties to help secure responsive, cost effective and risk mitigated supply chains to compete on a world stage. This should not wait until a drug has been registered, but should start as early as possible in the development process and before registration or clinical trials. The author suggests that CMC (chemistry manufacturing controls) drug development must reset the line of sight – from supply of drug to the clinic and gaining a registration, to the building of a patient value stream. Capable processes and suppliers, streamlined logistics, flexible plant and equipment, shorter cycle times, effective flow of information and reduced waste. All these factors can and should be addressed at the CMC development stage.

Kooperationsplattformen F R Das Supply Chain Management

Author: Ronald Poppe
Publisher: Springer-Verlag
ISBN: 3658163690
Size: 43.59 MB
Format: PDF, Docs
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Auf der Basis von SCM-Referenzmodellen der Automobil-, Konsumgüter- und Logistikindustrie entwickelt Ronald Poppe systematisch eine SCM-Kooperationsplattform als ganzheitliches und praktisch umsetzbares Gestaltungsmodell für die kooperative Koordination der Supply Chain. Der Autor legt die Machbarkeit und den Nutzen über eine beschreibende Fallstudie der pharmazeutischen Industrie dar. Weiterhin werden die abgeleiteten Gestaltungsempfehlungen für den kombinativen Einsatz struktureller, technokratischer und informationeller Koordinationsinstrumente zusammen mit weiteren Praxisfällen konkretisiert.

Clinical Trials In Neurology

Author: Bernard Ravina
Publisher: Cambridge University Press
ISBN: 1107376572
Size: 65.35 MB
Format: PDF
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Translating laboratory discoveries into successful therapeutics can be difficult. Clinical Trials in Neurology aims to improve the efficiency of clinical trials and the development of interventions in order to enhance the development of new treatments for neurologic diseases. It introduces the reader to the key concepts underpinning trials in the neurosciences. This volume tackles the challenges of developing therapies for neurologic disorders from measurement of agents in the nervous system to the progression of clinical signs and symptoms through illustrating specific study designs and their applications to different therapeutic areas. Clinical Trials in Neurology covers key issues in Phase I, II and III clinical trials, as well as post-marketing safety surveillance. Topics addressed include regulatory and implementation issues, outcome measures and common problems in drug development. Written by a multidisciplinary team, this comprehensive guide is essential reading for neurologists, psychiatrists, neurosurgeons, neuroscientists, statisticians and clinical researchers in the pharmaceutical industry.

Find It File It Flog It

Author: Hedley Rees
Publisher: Wordcatcher Publishing
ISBN: 1911265733
Size: 19.73 MB
Format: PDF, Kindle
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WARNING! Your life may be at risk due to the greed and avarice of pharma companies who are putting dangerous drugs on the market. Big Pharma is a money-making machine that extracts cash out of unwary investors. Producing a drug that hits the shelves involves millions of dollars of wasted money. And it's a cycle that repeats over, and over again.

The Sage Encyclopedia Of Pharmacology And Society

Author: Sarah E. Boslaugh
Publisher: SAGE Publications
ISBN: 1506301320
Size: 17.82 MB
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The SAGE Encyclopedia of Pharmacology and Society explores the social and policy sides of the pharmaceutical industry and its pervasive influence in society. While many technical STM works explore the chemistry and biology of pharmacology and an equally large number of clinically oriented works focus on use of illegal drugs, substance abuse, and treatment, there is virtually nothing on the immensely huge business (“Big Pharma”) of creating, selling, consuming, and regulating legal drugs. With this new Encyclopedia, the topic of socioeconomic, business and consumer, and legal and ethical issues of the pharmaceutical industry in contemporary society around the world are addressed. Key Features: 800 signed articles, authored by prominent scholars, are arranged A-to-Z and published in a choice of electronic or print formats Although arranged A-to-Z, a Reader's Guide in the front matter groups articles by thematic areas Front matter also includes a Chronology highlighting significant developments in this field All articles conclude with Further Readings and Cross References to related articles Back matter includes an annotated Resource Guide to further research, a Glossary, Appendices (e.g., statistics on the amount and types of drugs prescribed, etc.), and a detailed Index The Index, Reader’s Guide, and Cross References combine for search-and-browse capabilities in the electronic edition The SAGE Encyclopedia of Pharmacology and Society is an authoritative and rigorous source addressing the pharmacology industry and how it influences society, making it a must-have reference for all academic libraries as a source for both students and researchers to utilize.

Patient Focused Network Integration In Biopharma

Author: Robert Handfield
Publisher: CRC Press
ISBN: 1482218984
Size: 47.46 MB
Format: PDF, Kindle
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The biopharmaceutical industry as we know it today is going through a massive upheaval as a result of the uncertainty of healthcare reform and increasing regulatory pricing pressure. A wake-up call to all sectors of the healthcare value chain, Patient-Focused Network Integration in BioPharma: Strategic Imperatives for the Years Ahead explores patient-focused network integration as quite possibly the only way for organizational evolution to occur. The book discusses how to align enterprises with the patient at the center. It details the historical context of the biopharmaceutical value chain and the current set of challenges facing the industry, and then details the author’s unique and sustainable agenda for change. The book traces the critical but often ignored relationships between hospitals, insurance companies, biopharma manufacturers, government regulators, and clinical scientists. For too long, these parties have been operating in a void, without recognizing the interconnectedness of their objectives, even though these objectives are often competing and misaligned. This book points out the gaps that exist and develops a set of recommendations regarding disease treatments, clinical development of new products, and collaboration between these players that can result in a sustainable solution to the healthcare mess. Each chapter can be viewed as an independent essay, in that it deals with a specific dimension of the healthcare value chain. However, together they provide an integrated discussion on how to begin the task of creating an integrated value chain network for healthcare. The book begins with the patient, and then works its way back down the value chain, all the way to the drug development and clinical trials stage of the value chain. The common thread throughout the chapters is the emphasis on collaboration, strategic alignment, and a focus on delivering value to the end patient. Very simply, all parties in the healthcare value chain network must align their strategic planning to derive innovation solutions. It is only through true collaboration and aligned thinking that the parties in the drug development, distribution, insurance payors, and hospital provider network can deal with the incredible complexity and massive challenges that face the industry. The book provides a compelling maturity model that enables readers to gauge the level of network integration their enterprise is at today, and where they need to move in the future.

Mysap Supply Chain Management

Author: Erik Neumann
Publisher: GRIN Verlag
ISBN: 3638273997
Size: 24.90 MB
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Studienarbeit aus dem Jahr 2003 im Fachbereich Informatik - Wirtschaftsinformatik, Note: 2.0, Hochschule für Technik und Wirtschaft Berlin (Fachhochschule), Veranstaltung: AWE Logistik & Wirtschaftsverkehr, Sprache: Deutsch, Abstract: Das vorliegende Script befasst sich mit den Grundlagen der Güter- und Informationslogistik und dem SAP Modul mySAP SCM im Rahmen der Lehrveranstaltung Logistik und Wirtschaftsverkehr. Die Bildung von zwischenbetrieblichen Kooperationen wird für die beteiligten Akteure immer häufiger ein Instrument der Verbesserung ihrer Wettbewerbsfähigkeit und ihrer Wettbewerbsposition in einer globalen Weltwirtschaft. Diese Tendenz lässt sich auch in der Logistik beobachten. So sind in einer Logistikkette mehrere „Player“ beteiligt : Lieferanten, Hersteller, Handelsunternehmen, Logistikdienstleister und schließlich der Endkunde. Im Vordergrund des Supply Chain Management steht die übergreifende Optimierung der Güter- und Informationsflüsse. Zur Unterstützung logischer Prozesse bietet die SAP AG für die Beteiligten der Logistikkette unterschiedliche Systeme mit unterschiedlichen Funktionalitäten an. Diese reichen von der Abbildung der logischer Grundfunktionen im R/3 System wie Versand und Vertrieb ( Modul SD ), sowie Materialwirtschaft ( Modul MM ) über EDI und Workflow Management bis hin zur Organisation zwischenbetreiblicher Geschäftsprozesse über das Internet. Einen Teil dazu trägt die Supply Chain Management Initiative bei, die unterschiedliche Komponenten zur Optimierung der Logistikkette enthält. Im Zentrum des vorliegenden Scripts stehen zwischenbetriebliche Geschäftsprozesse und Kooperationen in der Logistikkette vor dem Hintergrund einer Untersuchung von Möglichkeiten und Grenzen im Einsatz von SAP Systemen.