Readers will be able to effectively and efficiently design and interpret findings from post-authorization safety studies with the goal of improving the benefit-risk balance of a drug in order to optimize patient safety.
- Discusses all types of observational studies in post-marketing drug safety assessment, from spontaneous reporting systems, to pragmatic trials, with examples from real-world settings
- Presents various types of post-authorization safety studies
- Offers solutions to the common challenges in the design and conduct of these studies
- Highlights active surveillance programs, including common data models for rapid signal detection of drug safety issues
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