Clearly explaining what to expect from the study is critical to ensuring potential study participants are truly informed about their participation—this is important no matter what language they speak. In this webinar, Roberto Torres, Director of Business Development at the Puerto Rico Consortium for Clinical Investigation, and Michele Russell-Einhorn, Vice President of Human Subject Protection Services and Institutional Official at Schulman IRB, discuss the regulatory requirements involved in enrolling a non-English speaking study participant. They will also discuss practical considerations for sites working with non-English speaking participants during the informed consent process.
Who Should Attend
Certificates of attendance are available for this event. This presentation may qualify for continuing education credits.