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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 var...
| Clasificación: | Libro Electrónico |
|---|---|
| Autor principal: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Hoboken :
CRC Press,
2010.
|
| Colección: | Chapman & Hall/CRC Biostatistics Series, 35
|
| Temas: | |
| Acceso en línea: | Texto completo |
MARC
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| 100 | 1 | |a Peace, Karl E. | |
| 245 | 1 | 0 | |a Clinical Trial Methodology. |
| 260 | |a Hoboken : |b CRC Press, |c 2010. | ||
| 300 | |a 1 online resource (422 pages) | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 490 | 0 | |a Chapman & Hall/CRC Biostatistics Series, 35 | |
| 505 | 0 | |a Front cover; Contents; Preface; Chapter 1: Overview of Clinical Trial Methodology; Chapter 2: Overview of the Drug Development Processand Regulation of Clinical Trials; Chapter 3: Ethical Considerations in the Designand Conduct of Clinical Trials; Chapter 4: Sample Size Considerations in ClinicalTrials Pre-Market Approval; Chapter 5: Sequential, Group Sequential, StochasticCurtailment, and Adaptive DesignProcedures in Clinical Trials; Chapter 6: Biostatistical Aspects of the Protocol; Chapter 7: The Statistical Analysis Plan; Chapter 8: Pooling of Data from Multicenter Clinical Trials. | |
| 505 | 8 | |a Chapter 9: Validity of Statistical InferenceChapter 10: Bioequivalence Clinical Trials; Chapter 11: Dose and Frequency Determinationfrom Phase II Clinical Trials in StressTest-Induced Angina; Chapter 12: Confirmation of Clinically Optimal Dosingin the Treatment of Duodenal Ulcers:A Phase III Dose Comparison Trial; Chapter 13: Pivotal Proof-of-Efficacy Clinical Trialsin the Prevention of NANSAID-InducedGastric Ulcera. | |
| 520 | |a 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 various clinical trials. | ||
| 588 | 0 | |a Print version record. | |
| 590 | |a ProQuest Ebook Central |b Ebook Central Academic Complete | ||
| 650 | 0 | |a Clinical trials. | |
| 650 | 0 | |a Drugs |x Testing. | |
| 650 | 2 | |a Clinical Trials as Topic | |
| 650 | 6 | |a Études cliniques. | |
| 650 | 6 | |a Médicaments |x Essais cliniques. | |
| 650 | 7 | |a Clinical trials |2 fast | |
| 650 | 7 | |a Drugs |x Testing |2 fast | |
| 758 | |i has work: |a Clinical trial methodology (Text) |1 https://id.oclc.org/worldcat/entity/E39PCG9XJCgFVtBFFC4vV8y9cK |4 https://id.oclc.org/worldcat/ontology/hasWork | ||
| 776 | 0 | 8 | |i Print version: |a Peace, Karl E. |t Clinical Trial Methodology. |d Hoboken : CRC Press, ©2010 |z 9781584889175 |
| 856 | 4 | 0 | |u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=555711 |z Texto completo |
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