PROCEDURE The test is often carried out either in 5 authentic containers if adequate quantity of product or service is on the market in Each and every container along with the solution container could be entered aseptically (i.e., needle and syringe by an elastomeric rubber stopper), or in 5 sterile, capped bacteriological containers of suited meas
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Remember to activate cookies with your browser settings so as to practical experience the full scope of this Web page. Jump to key navigationsix. Establishing the reliability of pharmaceutical water purification, storage, and distribution systems requires demonstrating control of the procedure by way of an acceptable duration of checking and observ