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.?
687what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
861What is the formula for relative diffrence for standard solution in solution stability in validation?
766[3/30, 13:29] Manoj P Venkatpurwar: How hplc column selection according to structure? How mobile phase buffer selection on molecule structure?
726in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
794If change in specification which parameter require to do for validation? if change in chromtographic condition then which parameter? if api change then which parameter? if change composition then which parameter? if old method not work out then whicj parameter? if additional one impurity added then which parameter of validation require to do on above each conditions? elaborate separately
823Post New Analytical Chemistry Questions
what is the extinction coefficient for Indomethacin or at 319nm wave length.
How to choose the which salt is suitable for mobilephase
We use hicrome 10 cxs column in hplc analysis....pls tell me.. what is the meaning of 10 cxs?
In rs method development when we are going area normalization method to dilute standard method?
What is rs test why we are performing rs test?
if your impurity coeluting with each other in that situation how require to set specification? is it acceptable?
for inorganic molecules require to do RS, Assay and disso?
Why sometime potassium ortho phosphate mix with acetone use for sample preparation for hplc
some product having water content method with pyridine and ethylene glycol mixture instead of methanol? how they are selecting and methanol is not suitable solvent how ?
from where i get mortar pastle for glass bottle crush? it's required for testing of it?
what is difference between UV - VISIBLE MODEL NO like 1600,1601,1700 etc ? plz explain me
CAN WE DETERMINE THE PEAK PURITY IN GAS CHROMATOGRAPHY ANALYSIS?
in each media we require to use SLS? how to proceed?
how you establish the LOQ?