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Non-inferiority Trials: Practical Issues and Current Regulatory Perspectives

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This webinar will examine and highlight differences among non-inferiority (NI) trials, equivalence, and superiority study objectives and designs. It will also review current FDA guidance for NI clinical studies.

Instructor: Rita Hanover
Product ID: 702476

Course "Non-inferiority Trials: Practical Issues and Current Regulatory Perspectives" has been pre-approved by RAPS as eligible for up to 1 RAC credits towards a participant's RAC recertification upon full completion.

Why Should You Attend:

Basic non-inferiority (NI) clinical study designs appear to provide a straight-forward approach for evaluating whether a new drug or medical device is an appropriate substitute or replacement for a current standard treatment. In these studies the typical comparison is between a new drug and an active control with the goal of demonstrating that the new drug is “not inferior” to the standard treatment by “too large” a margin. Traditional approaches to demonstrating NI of a new drug amounted to a simple acceptance of the null hypothesis of no difference between that drug and an active control, but these are currently recognized as inadequate to support a claim of NI.

This webinar will examine the philosophy and assumptions underlying NI trials by highlighting the differences among NI, equivalence, and superiority trials with regard to basic clinical study designs and appropriate hypothesis tests, power and sample size, and conceptual and statistical analysis differences. We will conclude with a review of current FDA guidance for NI clinical studies.

Areas Covered in the Seminar:

Who Will Benefit:

Professionals who will benefit from this webinar include:

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)

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Refund Policy
Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance.
ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

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Training Options Training Duration = 60 Min
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Recorded Link and Ref. material will be available in My CO Section
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