Problem:
Based on the information provided below and discussed in Week 5 Introduction to Clinical Regulation and Essential Documentation, submit a discussion board post providing information on a particular Institutional Review Board (IRB)Visit the Office for Human Research Protections database and select an Active IRB. For the IRB you have selected, provide the IRB name and number, location, and FWA number. Visit the IRB's website and describe the information you are able to find. If possible, provide a brief description of the type of research your selected IRB oversees (e.g. oncology, pediatric, vaccines, phase I, phase III), IRB-specific review schedule or timeframes, and any IRB-specific forms or documentation required for review.