I will never get proof before Ad Com. I can notify HHS OIG of already delayed meddling of generics into NCE determinations and request an investigation into PDUFA delay. Fact: PDUFA was delayed. Where the investigation should start?: Hikma interests into R-I sNDA after discovery has been closed in patent suit.
Opinion on my proposal to Woodcock?
I will requests documents from Amarin for the above complaint.