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Answer Posted / sreekanth
NANO3
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How we can identify process related and degradation impurity in single method with short period?
identification is for unknown? qualification for known? reporting for LOQ?
if you have given one product then how you determine the impurity in that?
before starting analytical method valodation what you checking? and how giving preference to start validation?
1)What's the meaning of Absorption,give a example. 2)What's the meaning of Adsorption,give a example. 2)what is the difference between Absorption and Adsorption.
why sre you used Potassium hydrogen phthalate in standarisation of 1N NaOH and 0.1 N Perchloric Acid?
if rsd failed then what require to do?
what parameters we will consider while developing a HPLC method and how we confirm our HPLC method is valid?
If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?
IS THERE ANY EQUIPMENT TO CHECK AND CALCULATE THE POLARITY OF A LIQUID?
How they found 1mL of K.F reagent is equivalent to 5mg of water and if we change the composition of K.F reagent, is it can neutralize more amount of water?
WHY pKa value is more important than pH value of the mobile phase in HPLC?
Did anybody have method for acetyl cysteine effervescnce tablet
Why only Copper standard is used to calibrate Atomic Absorption spectrophotometer?
What is the difference between Discriminating media and DPDM(Dissolution Profile with Different Media)
