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
1 2693why kbr is used for pellet preparation in ir spectroscopy, give the reasons? why kbr shows zero dipole moment?
6 15884
What forms the basis for colorimetric determination?
Give the others form of iron ore.
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
What is the difference between Discriminating media and DPDM(Dissolution Profile with Different Media)
if your product is soluble in 0.1n hcl and water then which you choose as media from these 2 media?
why we use Dichlorobenzene.nitrobezine.t-butyldi sulhate.for calibration of gc Head space
which gas is used in preaparation of bit salt
Explain acid gas?
How to decide assay range for non pharmacopeial API analysis by HPLC? Could you give me any reference for same e.g Guidelines or Paper publications?
How many electrons does benzene have?
What is the accepted microbial load in APIs as per USP.........?
what are risk assement in the analytical qbd?
How we performed the force degradation for drug substance, is any specific guideline is available for each parameter(Acidic, basic, oxidation,heat)? what conditions you mentained for above parameters.
If combination product how require to identify which imp is of which api?
why sre you used Potassium hydrogen phthalate in standarisation of 1N NaOH and 0.1 N Perchloric Acid?