Prisbevakning
Få notis vid prissänkningAv: Lawrence M. Friedman, Curt Furberg, David L. DeMets, David Reboussin, Christopher B. Granger
Lägsta pris
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Butiken med lägst pris i prislistan på boksidan just nu.
This is the fifth edition of a very successful textbook on clinical trials methodology, written by recognized leaders who have long and extensive experience in all areas of clinical trials. The three authors of the first four editions have been joined by two others who add great expertise. Most chapters have been revised considerably from the fourth edition. A chapter on regulatory issues has been included and the chapter on data monitoring has been split into two and expanded. Many contemporary clinical trial examples have been added. There is much new material on adverse events, adherence, issues in analysis, electronic data, data sharing and international trials. This book is intended for the clinical researcher who is interested in designing a clinical trial and developing a protocol. It is also of value to researchers and practitioners who must critically evaluate the literature of published clinical trials and assess the merits of each trial and the implications for the care and treatment of patients. The authors use numerous examples of published clinical trials to illustrate the fundamentals. The text is organized sequentially from defining the question to trial closeout. One chapter is devoted to each of the critical areas to aid the clinical trial researcher. These areas include pre-specifying the scientific questions to be tested and appropriate outcome measures, determining the organizational structure, estimating an adequate sample size, specifying the randomization procedure, implementing the intervention and visit schedules for participant evaluation, establishing an interim data and safety monitoring plan, detailing the final analysis plan and reporting the trial results according to the pre-specified objectives. Although a basic introductory statistics course is helpful in maximizing the benefit of this book, a researcher or practitioner with limited statistical background would still find most if not all the chapters understandable and helpful. While the technical material has been kept to a minimum, the statistician may still find the principles and fundamentals presented in this text useful. This book has been successfully used for teaching courses in clinical trial methodology. Format Inbunden Omfång 550 sidor Språk Engelska Förlag Springer International Publishing AG Utgivningsdatum 2015-09-12 ISBN 9783319185385
Okej pris
Adlibris
10 kr dyrare
Rör sig ofta
Författare
Lawrence M. Friedman, Curt Furberg, David L. DeMets, David Reboussin, Christopher B. Granger
Författare
Lawrence M. Friedman, Curt Furberg, David L. DeMets, David Reboussin, Christopher B. Granger
Förlag
Springer
Utgivningsår
2015
Format
Inbunden
Sidantal
550
Språk
Engelska
Fysiska detaljer
illustrations
Dewey
610.72/4
ISBN
9783319185385
Av: Lawrence M. Friedman, Curt Furberg, David L. DeMets, David Reboussin, Christopher B. Granger
Lägsta pris
Vi har hittat boken hos 2 butiker med verifierade priser — alla är partnerbutiker som vi får provision från när du klickar på ”Visa hos butik”. Vissa butiker visas som extern länk utan pris — priset ser du först hos butiken. Priset för dig är detsamma. Frakt kan tillkomma och varierar mellan butiker och leveranssätt — kontrollera alltid aktuellt pris och leveransvillkor hos butiken innan du slutför köpet.
Skriver du om boken på en blogg eller sajt? .
Priset har nyligen gått ner jämfört med butikens eget tidigare pris.
Det lägsta priset vi sett för boken sedan Booki började mäta.
Billigaste butiken ligger under de övriga butikernas medianpris just nu — en jämförelse mellan butiker, inte ett prisfall över tid.
Butiken med lägst pris i prislistan på boksidan just nu.
This is the fifth edition of a very successful textbook on clinical trials methodology, written by recognized leaders who have long and extensive experience in all areas of clinical trials. The three authors of the first four editions have been joined by two others who add great expertise. Most chapters have been revised considerably from the fourth edition. A chapter on regulatory issues has been included and the chapter on data monitoring has been split into two and expanded. Many contemporary clinical trial examples have been added. There is much new material on adverse events, adherence, issues in analysis, electronic data, data sharing and international trials. This book is intended for the clinical researcher who is interested in designing a clinical trial and developing a protocol. It is also of value to researchers and practitioners who must critically evaluate the literature of published clinical trials and assess the merits of each trial and the implications for the care and treatment of patients. The authors use numerous examples of published clinical trials to illustrate the fundamentals. The text is organized sequentially from defining the question to trial closeout. One chapter is devoted to each of the critical areas to aid the clinical trial researcher. These areas include pre-specifying the scientific questions to be tested and appropriate outcome measures, determining the organizational structure, estimating an adequate sample size, specifying the randomization procedure, implementing the intervention and visit schedules for participant evaluation, establishing an interim data and safety monitoring plan, detailing the final analysis plan and reporting the trial results according to the pre-specified objectives. Although a basic introductory statistics course is helpful in maximizing the benefit of this book, a researcher or practitioner with limited statistical background would still find most if not all the chapters understandable and helpful. While the technical material has been kept to a minimum, the statistician may still find the principles and fundamentals presented in this text useful. This book has been successfully used for teaching courses in clinical trial methodology. Format Inbunden Omfång 550 sidor Språk Engelska Förlag Springer International Publishing AG Utgivningsdatum 2015-09-12 ISBN 9783319185385
Okej pris
Adlibris
10 kr dyrare
Rör sig ofta
Författare
Lawrence M. Friedman, Curt Furberg, David L. DeMets, David Reboussin, Christopher B. Granger
Författare
Lawrence M. Friedman, Curt Furberg, David L. DeMets, David Reboussin, Christopher B. Granger
Förlag
Springer
Utgivningsår
2015
Format
Inbunden
Sidantal
550
Språk
Engelska
Fysiska detaljer
illustrations
Dewey
610.72/4
ISBN
9783319185385
Inbunden · 2015 · Engelska
Lawrence M. Friedman, Curt Furberg, David L. DeMets, David Reboussin, Christopher B. Granger
ISBN 9783319185385 jämförs hos alla butiker
This is the fifth edition of a very successful textbook on clinical trials methodology, written by recognized leaders who have long and extensive experience in all areas of clinical trials. The three authors of the first four editions have been joined by two others who add great expertise. Most chapters have been revised considerably from the fourth edition. A chapter on regulatory issues has been included and the chapter on data monitoring has been split into two and expanded. Many contemporary clinical trial examples have been added. There is much new material on adverse events, adherence, issues in analysis, electronic data, data sharing and international trials. This book is intended for the clinical researcher who is interested in designing a clinical trial and developing a protocol. It is also of value to researchers and practitioners who must critically evaluate the literature of published clinical trials and assess the merits of each trial and the implications for the care and treatment of patients. The authors use numerous examples of published clinical trials to illustrate the fundamentals. The text is organized sequentially from defining the question to trial closeout. One chapter is devoted to each of the critical areas to aid the clinical trial researcher. These areas include pre-specifying the scientific questions to be tested and appropriate outcome measures, determining the organizational structure, estimating an adequate sample size, specifying the randomization procedure, implementing the intervention and visit schedules for participant evaluation, establishing an interim data and safety monitoring plan, detailing the final analysis plan and reporting the trial results according to the pre-specified objectives. Although a basic introductory statistics course is helpful in maximizing the benefit of this book, a researcher or practitioner with limited statistical background would still find most if not all the chapters understandable and helpful. While the technical material has been kept to a minimum, the statistician may still find the principles and fundamentals presented in this text useful. This book has been successfully used for teaching courses in clinical trial methodology. Format Inbunden Omfång 550 sidor Språk Engelska Förlag Springer International Publishing AG Utgivningsdatum 2015-09-12 ISBN 9783319185385
Okej pris
Adlibris
10 kr dyrare
Rör sig ofta
Författare
Lawrence M. Friedman, Curt Furberg, David L. DeMets, David Reboussin, Christopher B. Granger
Förlag
Springer
Utgivningsår
2015
Format
Inbunden
Sidantal
550
Språk
Engelska
ISBN
9783319185385
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