Chengxing (27 resultados)
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Librería: Rarewaves.com USA, London, LONDO, Reino UnidoRarewaves.com USA
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EUR 103,39
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EUR 100,51
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Hardback. Condición: New.
Master Protocol Clinical Trials for Evidence Generation : Strategies, Designs, Operations, and Case Studies
Lu, Ruixiao (EDT); Ye, Jingjing (EDT); Lu, Chengxing (EDT); Wang, William (EDT)
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Librería: GreatBookPrices, Columbia, MD, Estados Unidos de AmericaGreatBookPrices
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EUR 180,88
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Master Protocol Clinical Trials for Evidence Generation : Strategies, Designs, Operations, and Case Studies
Lu, Ruixiao (EDT); Ye, Jingjing (EDT); Lu, Chengxing (EDT); Wang, William (EDT)
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Librería: GreatBookPrices, Columbia, MD, Estados Unidos de AmericaGreatBookPrices
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EUR 187,07
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Librería: California Books, Miami, FL, Estados Unidos de AmericaCalifornia Books
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EUR 189,43
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Librería: Majestic Books, Hounslow, Reino UnidoMajestic Books
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EUR 191,89
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Master Protocol Clinical Trials for Evidence Generation : Strategies, Designs, Operations, and Case Studies
Lu, Ruixiao (EDT); Ye, Jingjing (EDT); Lu, Chengxing (EDT); Wang, William (EDT)
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Librería: GreatBookPricesUK, Woodford Green, Reino UnidoGreatBookPricesUK
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EUR 180,24
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Master Protocol Clinical Trials for Evidence Generation : Strategies, Designs, Operations, and Case Studies
Lu, Ruixiao (EDT); Ye, Jingjing (EDT); Lu, Chengxing (EDT); Wang, William (EDT)
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EUR 219,87
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Librería: THE SAINT BOOKSTORE, Southport, Reino UnidoTHE SAINT BOOKSTORE
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Hardback. Condición: New. New copy - Usually dispatched within 4 working days.
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Librería: PBShop.store UK, Fairford, GLOS, Reino UnidoPBShop.store UK
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Librería: Books Puddle, New York, NY, Estados Unidos de AmericaBooks Puddle
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EUR 221,60
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Librería: Biblios, frankfurt am main, HESSE, AlemaniaBiblios
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EUR 219,91
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Librería: moluna, Greven, Alemaniamoluna
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EUR 198,67
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Condición: New. Ruixiao LuDr. Ruixiao Lu is a recognized leader in the biotech and biopharma industry, currently serving as Vice President, Head of Biostatistics & Statistical Programming at Alumis Inc. She has held senior leadership roles at various c.
Master Protocol Clinical Trials for Evidence Generation: Strategies, Designs, Operations, and Case Studies
Lu, Ruixiao (Editor)/ Ye, Jingjing (Editor)/ Lu, Chengxing (Editor)/ Wang, William (Editor)
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Librería: Revaluation Books, Exeter, Reino UnidoRevaluation Books
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EUR 263,70
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Hardcover. Condición: Brand New. 480 pages. 9.18x6.12x9.45 inches. In Stock.
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Librería: AHA-BUCH GmbH, Einbeck, AlemaniaAHA-BUCH GmbH
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EUR 274,00
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Buch. Condición: Neu. Neuware - Drug development is at a crossroads. As personalized medicine and targeted therapies expand, traditional clinical trial models have become too slow, costly, and inefficient. To meet the urgent need for faster, reliable evidence generation and decision making, researchers and regulators alike have…turned to innovative trial designs. Among these, master protocols stand out as a transformative approach, allowing multiple therapies, disease subtypes, or objectives to be studied under a single, integrated framework. Proven successful in oncology, COVID-19, and beyond, they improve efficiency, reduce participant exposure to ineffective treatments, and accelerate meaningful outcomes with patient centric approach, prompting regulatory guidance and global adoption.This book provides a multidisciplinary exploration of master protocol clinical trials, blending clinical, statistical, regulatory, operational, economic insights and patients perspectives. It examines both opportunities and challenges in design and implementation, and provides in-depth summary and discussion on real-world examples such as I-SPY, ROAR, and RECOVERY. A practical guide for researchers, statisticians, regulators, and industry professionals, it demonstrates how master protocols can reshape drug development and bring innovative therapies to patients faster.¿ Provides comprehensive, theoretical and practical aspects for master protocol trials¿ Includes most recent development in the master protocol clinical trials¿ Covers broad topics such as trial designs, governance oversight, software implementation, database and data pipeline, multi-regional trials, risk and benefit with operational solutions, economic considerations, regulatory perspectives, patient engagement and diversity¿ Deep dives into numerous real world case studies, their underlying thinking, challenges and success.¿ Includes global perspective in multi-regional clinical development.
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Librería: Majestic Books, Hounslow, Reino UnidoMajestic Books
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EUR 111,35
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Librería: Books Puddle, New York, NY, Estados Unidos de AmericaBooks Puddle
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EUR 117,57
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Librería: Biblios, frankfurt am main, HESSE, AlemaniaBiblios
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EUR 112,75
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Condición: New. PRINT ON DEMAND.
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Librería: CitiRetail, Stevenage, Reino UnidoCitiRetail
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EUR 85,45
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Hardcover. Condición: new. Hardcover. Special Issue 'Additive Manufacturing of Fibre-Reinforced Polymer Composites' has 13 pioneering studies advancing AM-FRPCs. Covering aerospace, automotive, energy, sustainability, it presents integration of novel materials, process/structural innovations, smart functionalities. It shows AM e…nables complex geometries, multifunctional parts with tailored mechanical, thermal, sensing properties. Articles address interlaminar toughness, porosity, fibre misalignment via nano-fillers, hybrid reinforcements, optimised paths. The highlights include laser-induced graphene for real-time damage sensing; eco-friendly biocomposites (chem-treated natural fibres); and spatial 3D printing for low-density, high-strength trusses. Mechanical testing uses experimental/numerical methods: acoustic emission, digital image correlation, finite element simulation, and Taguchi optimisation. Integrating AI and neural networks in print tuning and performance prediction marks a shift to intelligent manufacturing. From boosting buckling in anisotropic grids to refining laser-sintering via thermal simulation, this Special Issue offers insights into current research and future opportunities in process control, defect mitigation, and in situ monitoring. It is a timely collection of scientific breakthroughs and engineering practices driving next-gen FRPCs via AM, aiding researchers, engineers, and designers using AM's unique high-performance composite advantages. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.
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Librería: AHA-BUCH GmbH, Einbeck, AlemaniaAHA-BUCH GmbH
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EUR 91,76
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Buch. Condición: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering.
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Librería: preigu, Osnabrück, Alemaniapreigu
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EUR 122,45
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Buch. Condición: Neu. Additive Manufacturing of Fibre Reinforced Polymer Composites | Buch | Englisch | 2025 | MDPI AG | EAN 9783725857319 | Verantwortliche Person für die EU: Libri GmbH, Europaallee 1, 36244 Bad Hersfeld, gpsr[at]libri[dot]de | Anbieter: preigu Print on Demand.
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Librería: Grand Eagle Retail, Bensenville, IL, Estados Unidos de AmericaGrand Eagle Retail
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EUR 212,00
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Hardcover. Condición: new. Hardcover. Drug development is at a crossroads. As personalized medicine and targeted therapies expand, traditional clinical trial models have become too slow, costly, and inefficient. To meet the urgent need for faster, reliable evidence generation and decision making, researchers and regulators alike… have turned to innovative trial designs. Among these, master protocols stand out as a transformative approach, allowing multiple therapies, disease subtypes, or objectives to be studied under a single, integrated framework. Proven successful in oncology, COVID-19, and beyond, they improve efficiency, reduce participant exposure to ineffective treatments, and accelerate meaningful outcomes with patient centric approach, prompting regulatory guidance and global adoption.This book provides a multidisciplinary exploration of master protocol clinical trials, blending clinical, statistical, regulatory, operational, economic insights and patients perspectives. It examines both opportunities and challenges in design and implementation, and provides in-depth summary and discussion on real-world examples such as I-SPY, ROAR, and RECOVERY. A practical guide for researchers, statisticians, regulators, and industry professionals, it demonstrates how master protocols can reshape drug development and bring innovative therapies to patients faster. Provides comprehensive, theoretical and practical aspects for master protocol trials Includes most recent development in the master protocol clinical trials Covers broad topics such as trial designs, governance oversight, software implementation, database and data pipeline, multi-regional trials, risk and benefit with operational solutions, economic considerations, regulatory perspectives, patient engagement and diversity Deep dives into numerous real world case studies, their underlying thinking, challenges and success. Includes global perspective in multi-regional clinical development This book provides a multidisciplinary exploration of master protocol clinical trials, blending clinical, statistical, regulatory, operational, economic insights and patients perspectives. It examines both opportunities and challenges in design and implementation, and provides in-depth summary and discussion on real-world examples. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.
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Librería: AussieBookSeller, Truganina, VIC, AustraliaAussieBookSeller
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EUR 187,60
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Hardcover. Condición: new. Hardcover. Drug development is at a crossroads. As personalized medicine and targeted therapies expand, traditional clinical trial models have become too slow, costly, and inefficient. To meet the urgent need for faster, reliable evidence generation and decision making, researchers and regulators alike… have turned to innovative trial designs. Among these, master protocols stand out as a transformative approach, allowing multiple therapies, disease subtypes, or objectives to be studied under a single, integrated framework. Proven successful in oncology, COVID-19, and beyond, they improve efficiency, reduce participant exposure to ineffective treatments, and accelerate meaningful outcomes with patient centric approach, prompting regulatory guidance and global adoption.This book provides a multidisciplinary exploration of master protocol clinical trials, blending clinical, statistical, regulatory, operational, economic insights and patients perspectives. It examines both opportunities and challenges in design and implementation, and provides in-depth summary and discussion on real-world examples such as I-SPY, ROAR, and RECOVERY. A practical guide for researchers, statisticians, regulators, and industry professionals, it demonstrates how master protocols can reshape drug development and bring innovative therapies to patients faster. Provides comprehensive, theoretical and practical aspects for master protocol trials Includes most recent development in the master protocol clinical trials Covers broad topics such as trial designs, governance oversight, software implementation, database and data pipeline, multi-regional trials, risk and benefit with operational solutions, economic considerations, regulatory perspectives, patient engagement and diversity Deep dives into numerous real world case studies, their underlying thinking, challenges and success. Includes global perspective in multi-regional clinical development This book provides a multidisciplinary exploration of master protocol clinical trials, blending clinical, statistical, regulatory, operational, economic insights and patients perspectives. It examines both opportunities and challenges in design and implementation, and provides in-depth summary and discussion on real-world examples. This item is printed on demand. Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability.
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Librería: CitiRetail, Stevenage, Reino UnidoCitiRetail
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EUR 222,05
Envío por EUR 43,24Se envía de Reino Unido a Estados Unidos de AmericaCantidad disponible: 1 disponibles
Hardcover. Condición: new. Hardcover. Drug development is at a crossroads. As personalized medicine and targeted therapies expand, traditional clinical trial models have become too slow, costly, and inefficient. To meet the urgent need for faster, reliable evidence generation and decision making, researchers and regulators alike… have turned to innovative trial designs. Among these, master protocols stand out as a transformative approach, allowing multiple therapies, disease subtypes, or objectives to be studied under a single, integrated framework. Proven successful in oncology, COVID-19, and beyond, they improve efficiency, reduce participant exposure to ineffective treatments, and accelerate meaningful outcomes with patient centric approach, prompting regulatory guidance and global adoption.This book provides a multidisciplinary exploration of master protocol clinical trials, blending clinical, statistical, regulatory, operational, economic insights and patients perspectives. It examines both opportunities and challenges in design and implementation, and provides in-depth summary and discussion on real-world examples such as I-SPY, ROAR, and RECOVERY. A practical guide for researchers, statisticians, regulators, and industry professionals, it demonstrates how master protocols can reshape drug development and bring innovative therapies to patients faster. Provides comprehensive, theoretical and practical aspects for master protocol trials Includes most recent development in the master protocol clinical trials Covers broad topics such as trial designs, governance oversight, software implementation, database and data pipeline, multi-regional trials, risk and benefit with operational solutions, economic considerations, regulatory perspectives, patient engagement and diversity Deep dives into numerous real world case studies, their underlying thinking, challenges and success. Includes global perspective in multi-regional clinical development This book provides a multidisciplinary exploration of master protocol clinical trials, blending clinical, statistical, regulatory, operational, economic insights and patients perspectives. It examines both opportunities and challenges in design and implementation, and provides in-depth summary and discussion on real-world examples. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.
