Product Title: Quantitative Evaluation of Safety in Drug Development: Design, Analysis and Reporting
Format:
Retail PDF,
Overview (Details, Topics and Speakers):
by Qi Jiang (Editor), H. Amy Xia (Editor)
State-of-the-Art Methods for Drug Safety Assessment
Responding to the increased scrutiny of drug safety in recent years, Quantitative Evaluation of Safety in Drug Development: Design, Analysis and Reporting explains design, monitoring, analysis, and reporting issues for both clinical trials and observational studies in biopharmaceutical product development. It presents the latest statistical methods for drug safety assessment.
The book’s three sections focus on study design, safety monitoring, and data evaluation/analysis. The book addresses key challenges across regulatory agencies, industry, and academia. It discusses quantitative approaches to safety evaluation and risk management in drug development, covering Bayesian methods, effective safety graphics, and risk-benefit evaluation.
Written by a team of experienced leaders, this book brings the most advanced knowledge and statistical methods of drug safety to the statistical, clinical, and safety community. It shares best practices and stimulates further research and methodology development in the drug safety area.
Product Details
- ISBN-13: 9781466555457
- Publisher: Taylor & Francis
- Publication date: 12/11/2014
- Series:Chapman & Hall/CRC Biostatistics Series , #67
- Pages: 382
Delivery Method
the Quantitative Evaluation of Safety in Drug Development: Design, Analysis and Reporting course/book will be provided for customer as download link. download link has NO Expiry and can be used anytime.
Contact Us
contact us to our email at support@med-cme.com or fill in the form below:
Reviews
There are no reviews yet.