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PROCEDURE The test might be carried out possibly in five initial containers if adequate quantity of product is available in Just about every container and the merchandise container can be entered aseptically (i.e., needle and syringe by means of an elastomeric rubber stopper), or in 5 sterile, capped bacteriological containers of acceptable measure
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This document discusses stability factors and apps of pharmaceutical suspensions. It notes that tiny particle size, raising viscosity, and preserving optimal temperature contribute to suspension balance.The big variance of your values in Fig. eleven for your titanium powder implies that FT4 is significantly less ideal for this substance than PFT a
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