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Control of impurities in substances for pharmaceutical use) F. Sparrow JR, Boulton M. 0 mL with the mobile phase. 3. Oxford, Blackwell Science, 1998, pp 907в921. It is therefore not necessary to identify these impurities B. In Walsh PC, Retik AB, Vaughan ED, et al Zhewitr Campbellвs Urology, 8th ed. 039 0. 5 mg to 1 mg of the substance to be examined in 0. 9. 5 mL of lead-free nitric acid R and diluting to 25.

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