It has everything to do with the discussion but if you're too simple minded to understand the connection, what would you like me to do? Dumb it down even more so you can grasp it?
Hmmmm, ok, so the FDA regulates pharmaceutical companies and makes them sterilize empty vials in aseptic processing. You're answer as to why the FDA mandates this is bc they do. Besides that being circular reasoning and an incredibly easy question to answer, you still can't answer it yet you're the sterility guru here to impart unfathomable wisdom on the forum lol?? I promise you it's not a trick question and the answer is simple enough.
If that simple question trips you up then it's like Sammy Sosa being struck out by a 12yo pitching underhand. You say it's erroneous only bc you fail to see the implications and line of reasoning.
Don't worry, it's abundantly clear you don't know anything and I'd never think you do.
Of course it does. If you can't see why then you really have no business in this discussion.
If you could choose between a bottle of Watson test cyp and some random UGL's test cyp and both are the same price, which you choose? My money is on you choosing the Watson bc you're assured strict quality, consistency, accuracy, and sterility. So the best way for a ugl to ensure its products are consistent, have accurate dosing, are sterile, etc is to try and mimick pharmaceutical procedures as closely as possible.