Clinical trials study design, endpoints and biomarkers, drug safety, FDA and ICH guidelines
Clinical Trials: Study Design, Endpoints and Biomarkers, Drug Safety, and FDA and ICH Guidelines is a practical guidebook for those engaged in clinical trial design. This book details the organizations and content of clinical trials, including trial design, safety, endpoints, subgroups, HRQoL, conse...
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| Main Author: | |
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| Format: | Book |
| Language: | English |
| Published: |
Amsterdam
Elsevier/AP
2012
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| Subjects: | |
| Online Access: | Click Here to View Status and Holdings. |
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The management of clinical trials 
Design and analysis of clinical trials with time-to-event endpoints