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Re: mrwrn2010 post# 23854

Tuesday, 08/21/2012 10:37:39 AM

Tuesday, August 21, 2012 10:37:39 AM

Post# of 403103
I think this is highly likely. It makes sense that the FDA would assign one or two people to handle all of Elites stuff. This allows them to become intimately familiar with the operations and BOD. They create one file and combine everything together based off the approval of the new location for manufacturing. Their case file is then sent to a second level for final review and bang, Elite gets multiple approvals all at the same time consistent with the new facility coming online into full operation.
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