Answer / kanakadurga

Cleaning validation for is the methodology used to assure
that a cleaning process removes residues of the active
pharmaceutical ingredients of the product manufactured in a
piece of equipment, the cleaning aids utilized in the
cleaning process and the microbialattributes. All residues
are removed to predetermined levels to ensure the quality of
the next product manufactured is not compromised by waste
from the previous product

What is the size of capillary tube used for analysing melting point?

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How to know HPLC column performance?

4 Answers   Meghmani Organics,

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why base line not starts from zero in gc?

1 Answers   Aurobindo, FDC, Reddy Labs,

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How much is the standard area for glc analysis

0 Answers  

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For standardization of volumetric solutions, acceptance limit for concentration is considered as 10% of nominal concentration and %RSD as NMT 0.2% (for appropriate no. of replicates). But , if %RSD has not met, what should be further action?

0 Answers  

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for heavy metal test lead used in which form pure form or any other form for preparation of lead standard sol

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why we are using benzene, anyline in acetic anhdride assay titration method?

0 Answers  

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which are the sizes of capsules?

0 Answers  

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why kf factor coming 0.5

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Why dst is used in kf for factor determination less than 1

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why we are performing residue on ignition?

2 Answers  

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If we have a kc is1*10^8 and the .kp 2*10^5 of reaction A------->B C------->D what is the volume of C?

0 Answers  

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