Answer Posted / sumit palta

its not about system suitability check .its about stability program in formulated drug product by following the ich guideline Q1D.

What is the diffrence in japan mkt requirement in analytical method validation over US?

725

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if identification threshold crosses the limits then what next step?

869

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how require to select dissolution media? what is discrimination?

792

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why we use Dichlorobenzene.nitrobezine.t-butyldi sulhate.for calibration of gc Head space

2269

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what is the procedure for cleaning of lenses of hatr accesory of ftir instrument?

2296

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What is the difference between Discriminating media and DPDM(Dissolution Profile with Different Media)

7549

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We use hicrome 10 cxs column in hplc analysis....pls tell me.. what is the meaning of 10 cxs?

1721

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what type of question will ask in the interview of lab chemist.

3323

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why sre you used Potassium hydrogen phthalate in standarisation of 1N NaOH and 0.1 N Perchloric Acid?

9803

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why holium oxide prepared in 10% HCLO4 SOLUTION

1462

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Did anybody have method for acetyl cysteine effervescnce tablet

2254

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In IR spectra, generally a molecule vibrates without apply emr or ir light?

1982

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pharma industries oriented

2249

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WHICH STANDARD WE USE IN SILICA ANALYSIS IN SILICA-GEL METHOD FOR SOLID SAMPLE

2134

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what is %labelled amount in content uniformity of dosage unit and its calculation?

5240

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