Given all this free time to think without being burdened by an FDA-induced rampaging SP.....
Can anyone outline what is required for 2012 European approval? I presume ACL (or whoever the partner happens to be) will want to submit an application ahead of time so that it's ready to go on ??? date.
Does RDY get first dibs at partnership?
Will EMEA approval include ACS?
Given the FDA wait.... perhaps it needs to start now!!
european approval
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