How to Vet an IRB: Expose and Fix Problems Before They Threaten Your Trial - Clinical Webinar By Com (Clinical)
Venue: Online Event
|Event Date/Time: Jan 20, 2011||End Date/Time: Jan 20, 2011|
The purpose of an IRB review is to assure, both in advance and by periodic review, that appropriate steps are taken to protect the rights and welfare of humans participating as subjects in a research study. To accomplish this purpose, IRBs review research protocols and related materials (e.g., informed consent documents and investigator brochures) to ensure protection of the rights and welfare of human subjects of research and to maximize the safety of subjects once they are enrolled in the project.
Submitting an IRB application right the first time requires a lot of attention to detail. Once a successful application is approved, it is important to keep up with the continuing requirements/submissions/changes etc. Attend this webinar to learn what the IRB is looking for and how to expose and fix problem before they threaten you trial and learn about the role and responsibilities of an efficient well rounded CRC.
Note: Use these promocode(117660) for 10% discount.