Event Detail
10 Tips for Submitting Human Subjects Protocols
October 22, 2012 - Palo Alto CA US
ComplianceOnline
referral@complianceonline.com
Phone: +1-650-620-3915
Fax: +1-650-963-2556
This webinar will provide tips on simple steps that may be taken by the investigator/research team in preparing his/her submission making it more IRB ready and therefore receiving less contingencies which in turn speed up the IRB review and approval process. Why Should You Attend: In conducting human subjects research, an investigator must send his/her protocol to the Institutional Review Board (IRB) for approval. Often seen as “black holes” that one submits to and awaits a determination, submitting a study to an IRB can seem like an arduous, daunting task. Because of this, investigators are always looking for tips that will make this process less mysterious and faster. This session is designed to remove some of the mystery of an IRB submission by providing tips on simple steps that may be taken by the investigator/research team in preparing his/her submission making it more IRB ready and therefore receiving less contingencies which in turn speed up the IRB review and approval process.