Advanced Superiority, Non-inferiority, or Equivalence Trials

This advanced webinar on clinical study design will explain the mechanics involved in design, execution, and analysis of alternate clinical trial designs - Superiority, Non-inferiority, and Equivalence Trials.

Who will Benefit:

Professionals who will benefit from this webinar include:

• Clinical Research Professionals
• Clinical Protocol Developers
• Clinical Study Managers
• Regulatory Managers
• Clinical Studies Directors
• Biostatisticians
• Anyone who seeks to design appropriate clinical investigations for supporting anticipated labeling for a new drug or medical device.

Instructor Profile:

Dr. Hanover, has worked in clinical research for over 30 years, as a Principal Investigator for studies funded by national agencies such as NIMH, Veteran’s Affairs, and DOD as well as various private pharmaceutical and medical device companies, as a Professor teaching research methods, biostatistics, and evidence-based medicine at the University of Utah School of Medicine, a Consultant to the Utah State Department of Health, and Director of Clinical Research for Techniscan Medical Systems. She has concurrently held consulting positions for such companies as Pherin Pharmaceuticals, Utah Cancer Specialists, Montgomery-Watson Environmental Engineering, and Planned Parenthood Federation of America. She earned a Regulatory Affairs Certification (RAC) in 2006 through RAPS, and is also a member of the Society of Clinical Research Associates (SOCRA), and the American Statistical Association (AMSTAT).