Answer / m

Linearity is showing the precisiness of results over the
specification range of LOQ or Lower concentration to 150%
or 200% of specification concentration and it is proved
that your method is precise over perticular concentration
selection range.

Answer / premraj behera

Based on the final concentration of the samples/standards
used for the validation of the method, homogeneity and
stability, the linearity plot (Concentration Vs Area) will
be plotted which covers the final concentration with ± 50%
range. so that analyzed concentration of the
samples/standards will fall within these range which is
acceptable.

Answer / shadab aga

WHAT IS THE SPECIFIC OPTICAL ROTATION OF SUGAR?

if rsd failed then what require to do?

0 Answers  

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which batch require to use for analytical method validation?

0 Answers  

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IS THERE ANYWHERE MENTION THAT THE RE PROCESS BATCH REQUIRE TO KEPT STABILITY STYDY

2 Answers   Nakoda Chemicals,

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what is mean by nitrosamine impurities?

0 Answers  

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How NMR spectra can be calibrated in presence or absence of TMS?

1 Answers  

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what is LC - MS ? What its wide use in cro/pharmaceutical Industry

4 Answers   Ranbaxy,

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What is the pilot-plant in pharma sector.

1 Answers   Dr Reddys,

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give tha clarity about peak purity concept

3 Answers   Aurobindo, Reliance Life Sciences,

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why water, methanol, ethanol ets solvents are used in UV SPECTRIPHOTOMETER for blank reading ?

7 Answers  

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Difference Between End Cap HPLC Column and Non End Cap Column

2 Answers  

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please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development

0 Answers   Pfizer,

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we are performed SOR for a particular product the limit is -6 to -10.We face particular bathes it is not meeting the specification.we performed diffrent instrument diffrent analyst we are getting diffrent diffrent results.solvent is dimethyl sulfoxide what could be the reasion

0 Answers   Cipla,

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