AN UNBIASED VIEW OF WATER SYSTEM QUALIFICATION IN PHARMA

Immediately after draining, this valve (the 2nd off with the system) is closed. If on the following day or begin-up with the Procedure the principal valve off of the circulating system is opened, then the non-sterile air remaining while in the pipe just after drainage would contaminate the system. The solution should be to pro-vide for operational

Acknowledged by the FDA as an advanced aseptic course of action for the packaging of sterile pharmaceutical liquids, blow-fill-seal technology is attaining rising acceptance by offering a substantial assurance of product sterility, eliminating the necessity for human intervention, bettering flexibility in container design and escalating course of a