RE:spammers working hard on this board, why are they here?re:
1. Development and validation of new analytical assays and in-process controls (complete)
2. Finalization of PPQ protocol (complete)
3. Manufacturing of additional conformance lots (complete)
4. Fill & Finish at external Contract Manufacturing Organization (“CMO”) (complete)
Show me where any of this is true. Show me a news release, show me a material filing.-- anything, anything at all will do as long as it is clear, unequivocal and disclosed.
Otherwise you are just a fkg liar.