Hi,
I would like to ask that:
1. How does the extent of effort in meeting 6 standards of regulatory model approval (use test, statistical quality, calibration, profit & loss attribution, validation & documentation) differ from a full internal model?
2. What are the integration options of partial internal model and their practicality? I am not looking for a very detailed treatment of this topic but more on high level understanding of realistic options available because I am unable to find more information for this topic than some regulatory texts which can be vastly different over time. What is the historic development that I have missed out?
Thank you.
Last edited by a moderator: Feb 5, 2018