CLINICAL COMPLIANCE 2011 - How to Vet an IRB: Expose and Fix Problems Before They Threaten Your Trial

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Category Clinical Webinar ,conference,event.

Deadline: January 20, 2011 | Date: January 20, 2011

Venue/Country: Palo Alto, U.S.A

Updated: 2010-12-23 19:30:50 (GMT+9)

Call For Papers - CFP

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.

Areas Covered in the Seminar:

IRB- Purpose, Use, Responsibilities.

IRB Application Process.

Single center trial vs. Multiple center trial.

Privately vs. Government sponsored trials.

Research Team and IRB.

IRB Document management.

How to prevent problems.