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Design and Analysis of Clinical Trials with Time-To-Event Endpoints (English, Karl E. Peace)
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Specifications
| Publisher | Chapman and Hall/CRC |
| Language | English |
| ISBN-13 | 9781420066395 |
| ISBN-10 | 1420066390 |
| Author | Karl E. Peace |
Product Description
Here on GlowMirror, you'll find Design and Analysis of Clinical Trials with Time-To-Event Endpoints filed under Research -- everything you need to know is covered below.
About the Book
Using time-to-event analysis methodology requires careful definition of the event, censored observation, provision of adequate follow-up, number of events, and independence or "noninformativeness" of the censoring mechanisms relative to the event. Design and Analysis of Clinical Trials with Time-to-Event Endpoints provides a thorough presentation of the design, monitoring, analysis, and interpretation of clinical trials in which time-to-event is…
ISBN: 9781420066395
Book Insights
What You'll Learn
- ·In-depth exploration of topics covered in Design and Analysis of Clinical Trials with Time-To-Event Endpoints
- ·Key concepts explained with clarity and practical examples
- ·Insights valuable for anyone studying or working in Research
Who Should Read This
Students and professionals interested in Research, as well as general readers looking to expand their knowledge.
Key Highlights
- ·Brand new physical book delivered across India
- ·15-day hassle-free return policy
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Is Design and Analysis of Clinical Trials with Time-To-Event Endpoints available in English?
Design and Analysis of Clinical Trials with Time-To-Event Endpoints is available in English on GlowMirror.
Who is the author of Design and Analysis of Clinical Trials with Time-To-Event Endpoints?
Design and Analysis of Clinical Trials with Time-To-Event Endpoints is authored by Karl E. Peace.
Who published Design and Analysis of Clinical Trials with Time-To-Event Endpoints?
Design and Analysis of Clinical Trials with Time-To-Event Endpoints is published by Chapman and Hall/CRC.
How many pages does Design and Analysis of Clinical Trials with Time-To-Event Endpoints have?
Page count information for Design and Analysis of Clinical Trials with Time-To-Event Endpoints is available in the specifications section of this page.
How long does it take to read Design and Analysis of Clinical Trials with Time-To-Event Endpoints?
At an average reading speed of 250 words per minute, reading Design and Analysis of Clinical Trials with Time-To-Event Endpoints takes a few hours to a few days depending on reading pace.
What is Design and Analysis of Clinical Trials with Time-To-Event Endpoints about?
About the Book
Using time-to-event analysis methodology requires careful definition of the event, censored observation, provision of adequate follow-up, number of events, and independence or "noninformativeness" of the censoring mechanisms relative to the event. Design and Analysis of Clinical Tri...
Is Design and Analysis of Clinical Trials with Time-To-Event Endpoints suitable for beginners?
Whether Design and Analysis of Clinical Trials with Time-To-Event Endpoints is suitable for beginners depends on your background in Research. Review the product description and specifications above for details on the target audience and difficulty level.
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Design and Analysis of Clinical Trials with Time-To-Event Endpoints is from the Chapman and Hall/CRC edition/year. Check the specifications section for full edition details.
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