Superiority, Non-inferiority, or Equivalence Trials: How, Why and When 2015 is a webinar that covers topics such as:
- Zeroing in on the specific clinical question to be asked
- Overview and comparison of NI, equivalence, and superiority study objectives and designs
- How to determine the appropriate interval of equivalence or acceptable "margin" of inferiority
- Choosing the appropriate design to answer the specific clinical question
- Risk of "BioCreep" and other controversies associated with these alternative approaches
- Appropriate hypothesis tests and statistical interpretation (for non-statisticians)
- FDA guidance and CONSORT considerations
Superiority, Non-inferiority, or Equivalence Trials: How, Why and When 2015 is intended for:
- Clinical Protocol Developers
- Clinical Research Professionals
- Regulatory Managers
- Clinical Study Managers
- Biostatisticians
- Clinical Studies Directors
