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my name is santhosh i cmpleted b.pharmacy in 2009 then i
went to uk in 2010 to pg diploma business management. after
i came back to india.. recently again apply to uk for
pharmaceutical analysis. they refused my visa you failed to
explain y u r change subject.
so plz ineed answer for y change the cource
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Answer Posted / falguni patel
U have to think before.. In between, u are on a wrong page. Nd also U could answered that person that i was change my sub, write now m choosing the right one.
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how you confirm the assay method?
how we can identify the impurity is coming below loq at transfering site?
which are the diffrent batches in the pharmaceuticals?
inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?
Why potassium dichromate is used in calibration of uv?
why multimedia dissolution require to do?
What is mean by PDR?
what is mean by covalidation
Which parameters require to do in tech transfer?
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?
Difference between hlaf and rlaf
I have compare C2H2-air and C2H2-N2O flame AAS on determination calcium. Both use same range of std to plot calibration curve. (2-6ppm) When i measure the sample with phosphate, KCl and LaCl, C2H2-N2O flame give false positive result, around 0.5ppm. When i measure the sample with phosphste, KCl and EDTA. C2H2-N2O flame also give 0.5ppm false positive. But both above mentioned sample would not give false positive when measured by C2H2-air flame. What is the reason?
What is delay volume?
How would you decide dissolution medium for NCE compound of class I drug
calibrtion procedue of LC-MS
