I just wanted to know - Filteration of the Drug product which is in the holding vessel is happening in the Grade C area with Laminar air flow Grade A? - Terminal sterilization And filteration and sterilization of Drug product which is in the holding vessel is happening in the Grade B area with Grade A laminar air flow - Asceptic sterilization Is this correct?
Sir, will you please answer my below question. Why ampoule products require sterilization and vial products for depyrogenation. Can we use depyrogenation tunnel for ampoule product
Also in the previous video you mentioned that cleaning of primary packaging materials such as vials is happened in the grade D area whereas now you're saying it's happening in the Grade C area? Can you confirm where it happens?
