Vi flyttar från butik till nätet - så funkar det framåt
Clinical Trial Methodology | 1:a upplagan
- Danskt band, Engelska, 2020
- Författare: Ding-Geng (Din) Chen, Karl E. Peace
- Betyg:
567
kr
Skickas inom 1-3 vardagar
Butikslager
Onlinelager
I lager hos leverantör
Fler utgåvor
-
Applied Meta-Analysis with R and Stata (2021)
2036 kr
-
Cure Models (2021)
995 kr
-
Bayesian Analysis of Infectious Diseases (2021)
1189 kr
-
Medical Risk Prediction Models (2021)
2261 kr
-
Design and Analysis of Animal Studies in Pharmaceutical Development (2020)
567 kr
-
Randomized Phase II Cancer Clinical Trials (2020)
567 kr
-
Benefit-Risk Assessment in Pharmaceutical Research and Development (2020)
567 kr
-
Bayesian Methods in Epidemiology (2020)
567 kr
-
Sample Size Calculations for Clustered and Longitudinal Outcomes in Clinical Research (2020)
504 kr
-
Inference Principles for Biostatisticians (2020)
567 kr
-
Medical Product Safety Evaluation (2020)
567 kr
-
Measures of Interobserver Agreement and Reliability (2020)
567 kr
-
Confidence Intervals for Proportions and Related Measures of Effect Size (2020)
567 kr
-
Randomized Clinical Trials of Nonpharmacological Treatments (2020)
567 kr
-
Controversial Statistical Issues in Clinical Trials (2020)
567 kr
-
Interval-Censored Time-to-Event Data (2020)
567 kr
-
Statistical Design and Analysis of Stability Studies (2020)
567 kr
-
Bayesian Methods for Measures of Agreement (2020)
567 kr
-
Design and Analysis of Bridging Studies (2020)
567 kr
-
Design and Analysis of Non-Inferiority Trials (2020)
567 kr
-
Advanced Bayesian Methods for Medical Test Accuracy (2020)
567 kr
-
Bayesian Analysis Made Simple (2020)
567 kr
-
Quantitative Methods for HIV/AIDS Research (2020)
567 kr
Beskrivning
Now viewed as its own scientific discipline, clinical trial methodology encompasses the methods required for the protection of participants in a clinical trial and the methods necessary to provide a valid inference about the objective of the trial. Drawing from the authors’ courses on the subject as well as the first author’s more than 30 years working in the pharmaceutical industry, Clinical Trial Methodology emphasizes the importance of statistical thinking in clinical research and presents the methodology as a key component of clinical research.
From ethical issues and sample size considerations to adaptive design procedures and statistical analysis, the book first covers the methodology that spans every clinical trial regardless of the area of application. Crucial to the generic drug industry, bioequivalence clinical trials are then discussed. The authors describe a parallel bioequivalence clinical trial of six formulations incorporating group sequential procedures that permit sample size re-estimation. The final chapters incorporate real-world case studies of clinical trials from the authors’ own experiences. These examples include a landmark Phase III clinical trial involving the treatment of duodenal ulcers and Phase III clinical trials that contributed to the first drug approved for the treatment of Alzheimer’s disease.
Aided by the U.S. FDA, the U.S. National Institutes of Health, the pharmaceutical industry, and academia, the area of clinical trial methodology has evolved over the last six decades into a scientific discipline. This guide explores the processes essential for developing and conducting a quality clinical trial protocol and providing quality data collection, biostatistical analyses, and a clinical study report, all while maintaining the highest standards of ethics and excellence.
From ethical issues and sample size considerations to adaptive design procedures and statistical analysis, the book first covers the methodology that spans every clinical trial regardless of the area of application. Crucial to the generic drug industry, bioequivalence clinical trials are then discussed. The authors describe a parallel bioequivalence clinical trial of six formulations incorporating group sequential procedures that permit sample size re-estimation. The final chapters incorporate real-world case studies of clinical trials from the authors’ own experiences. These examples include a landmark Phase III clinical trial involving the treatment of duodenal ulcers and Phase III clinical trials that contributed to the first drug approved for the treatment of Alzheimer’s disease.
Aided by the U.S. FDA, the U.S. National Institutes of Health, the pharmaceutical industry, and academia, the area of clinical trial methodology has evolved over the last six decades into a scientific discipline. This guide explores the processes essential for developing and conducting a quality clinical trial protocol and providing quality data collection, biostatistical analyses, and a clinical study report, all while maintaining the highest standards of ethics and excellence.
Om denna bok
Clinical Trial Methodology av Ding-Geng (Din) Chen och Karl E. Peace är en Danskt band bok med 420 sidor på Engelska. Detta är den 1:a upplagan som utgavs 2020.
Spara pengar – köp begagnad från Campusbokhandeln
Köp Clinical Trial Methodology begagnad från Campusbokhandeln och spara upp till 25% jämfört med nypris. Du kan bevaka den här boken så får du ett mail så fort vi får in den i lager som begagnad.
Genom att köpa & sälja begagnat sänker du kostnaden för studier både för dig och nästa student samtidigt som du gör nytta för klimatet.
Produktinformation
Kategori:
Medicin, vård & fysiologi
Bandtyp:
Danskt band
Språk:
Engelska
ISBN:
9780367577155
Upplaga:
1
Utgiven:
2020-06-30
Förlag:
Okänt
Sidantal:
420