Naitee Ting – författare
Visar alla böcker från författaren Naitee Ting. Handla med fri frakt och snabb leverans.
19 produkter
Fundamental Concepts for New Clinical Trialists
Häftad, 2021
831 kr
Lägg i varukorg
Fundamental Concepts for New Clinical Trialists describes the core scientific concepts of designing, data monitoring, analyzing, and reporting clinical trials as well as the practical aspects of trials not typically discussed in statistical methodology textbooks. The first section of the book …
Dose Finding in Drug Development
Av Naitee Ting
Inbunden, 2006
1853 kr
Lägg i varukorg
This book emphasizes dose selection issues from a statistical point of view. It presentsstatisticalapplicationsinthedesignandanalysisofdose–responsestudies. The importance of this subject can be found from the International Conference on Harmonization (ICH) E4 Guidance document. Establishing the …
Dose Finding in Drug Development
Av Naitee Ting
E-bok, 2006
1798 kr
Lägg i varukorg
This book emphasizes dose selection issues from a statistical point of view. It presentsstatisticalapplicationsinthedesignandanalysisofdose–responsestudies. The importance of this subject can be found from the International Conference on Harmonization (ICH) E4 Guidance document. Establishing the …
Fundamental Concepts for New Clinical Trialists
E-bok, 2015
874 kr
Lägg i varukorg
Fundamental Concepts for New Clinical Trialists describes the core scientific concepts of designing, data monitoring, analyzing, and reporting clinical trials as well as the practical aspects of trials not typically discussed in statistical methodology textbooks. The first section of the book …
Clinical Trials in the Era of Real-World Evidence
Av Jie Chen, Naitee Ting m. fl.
Häftad, 2026
1363 kr
Lägg i varukorg
Integrate RCTs and real-world evidence for stronger regulatory submissionsSince the passage of the 21st Century Cures Act, the landscape of clinical research has transformed dramatically. Today, the integration of real-world data (RWD) and real-world evidence (RWE) with traditional randomized …
Clinical Trials in the Era of Real-World Evidence
Av Feinan Lu, Naitee Ting m. fl.
E-bok, 2026
1678 kr
Lägg i varukorg
Integrate RCTs and real-world evidence for stronger regulatory submissions Since the passage of the 21st Century Cures Act, the landscape of clinical research has transformed dramatically. Today, the integration of real-world data (RWD) and real-world evidence (RWE) with traditional randomized …
Clinical Trials in the Era of Real-World Evidence
Av Feinan Lu, Naitee Ting m. fl.
E-bok, 2026
1642 kr
Lägg i varukorg
Integrate RCTs and real-world evidence for stronger regulatory submissions Since the passage of the 21st Century Cures Act, the landscape of clinical research has transformed dramatically. Today, the integration of real-world data (RWD) and real-world evidence (RWE) with traditional randomized …
Fundamental Concepts for New Clinical Trialists
Inbunden, 2015
1569 kr
Lägg i varukorg
Fundamental Concepts for New Clinical Trialists describes the core scientific concepts of designing, data monitoring, analyzing, and reporting clinical trials as well as the practical aspects of trials not typically discussed in statistical methodology textbooks. The first section of the book …
Dose Finding in Drug Development
Av Naitee Ting
Häftad, 2010
1684 kr
Lägg i varukorg
This book emphasizes dose selection issues from a statistical point of view. It presentsstatisticalapplicationsinthedesignandanalysisofdose–responsestudies. The importance of this subject can be found from the International Conference on Harmonization (ICH) E4 Guidance document. Establishing the …
Fundamental Concepts for New Clinical Trialists
E-bok, 2015
874 kr
Lägg i varukorg
Fundamental Concepts for New Clinical Trialists describes the core scientific concepts of designing, data monitoring, analyzing, and reporting clinical trials as well as the practical aspects of trials not typically discussed in statistical methodology textbooks. The first section of the book …
Design and Analysis of Subgroups with Biopharmaceutical Applications
Av Naitee Ting, Joseph C. Cappelleri m. fl.
Inbunden, 2020
1465 kr
Lägg i varukorg
This book provides an overview of the theories and applications on subgroups in the biopharmaceutical industry. Drawing from a range of expert perspectives in academia and industry, this collection offers an overarching dialogue about recent advances in biopharmaceutical applications, novel …
Design and Analysis of Subgroups with Biopharmaceutical Applications
Av (Din) Ding-Geng Chen, Shuyen Ho m. fl.
E-bok, 2020
1326 kr
Lägg i varukorg
This book provides an overview of the theories and applications on subgroups in the biopharmaceutical industry. Drawing from a range of expert perspectives in academia and industry, this collection offers an overarching dialogue about recent advances in biopharmaceutical applications, novel …
Design and Analysis of Subgroups with Biopharmaceutical Applications
Av Naitee Ting, Joseph C. Cappelleri m. fl.
Häftad, 2021
1017 kr
Lägg i varukorg
This book provides an overview of the theories and applications on subgroups in the biopharmaceutical industry. Drawing from a range of expert perspectives in academia and industry, this collection offers an overarching dialogue about recent advances in biopharmaceutical applications, novel …
Applied Statistics in Biomedicine and Clinical Trials Design
Selected Papers from 2013 ICSA/ISBS Joint Statistical Meetings
Inbunden, 2015
1690 kr
Lägg i varukorg
This volume is a unique combination of papers that cover critical topics in biostatistics from academic, government, and industry perspectives. The 6 sections cover Bayesian methods in biomedical research; Diagnostic medicine and classification; Innovative Clinical Trials Design; Modelling and Data …
Applied Statistics in Biomedicine and Clinical Trials Design
Selected Papers from 2013 ICSA/ISBS Joint Statistical Meetings
Av Yi Tsong, Naitee Ting m. fl.
E-bok, 2015
2174 kr
Lägg i varukorg
This volume is a unique combination of papers that cover critical topics in biostatistics from academic, government, and industry perspectives. The 6 sections cover Bayesian methods in biomedical research; Diagnostic medicine and classification; Innovative Clinical Trials Design; Modelling and Data …
Applied Statistics in Biomedicine and Clinical Trials Design
Selected Papers from 2013 ICSA/ISBS Joint Statistical Meetings
Häftad, 2016
1690 kr
Lägg i varukorg
This volume is a unique combination of papers that cover critical topics in biostatistics from academic, government, and industry perspectives. The 6 sections cover Bayesian methods in biomedical research; Diagnostic medicine and classification; Innovative Clinical Trials Design; Modelling and Data …
Phase II Clinical Development of New Drugs
Av Naitee Ting, Ding-Geng Chen m. fl.
Inbunden, 2017
1353 kr
Lägg i varukorg
This book focuses on how to appropriately plan and develop a Phase II program, and how to design Phase II clinical trials and analyze their data. It provides a comprehensive overview of the entire drug development process and highlights key questions that need to be addressed for the successful …
Phase II Clinical Development of New Drugs
Av Joseph C. Cappelleri, Shuyen Ho m. fl.
E-bok, 2017
1838 kr
Lägg i varukorg
This book focuses on how to appropriately plan and develop a Phase II program, and how to design Phase II clinical trials and analyze their data. It provides a comprehensive overview of the entire drug development process and highlights key questions that need to be addressed for the successful …
Phase II Clinical Development of New Drugs
Av Naitee Ting, Ding-Geng Chen m. fl.
Häftad, 2018
1353 kr
Lägg i varukorg
This book focuses on how to appropriately plan and develop a Phase II program, and how to design Phase II clinical trials and analyze their data. It provides a comprehensive overview of the entire drug development process and highlights key questions that need to be addressed for the successful …
