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.?
715what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
890What is the formula for relative diffrence for standard solution in solution stability in validation?
802[3/30, 13:29] Manoj P Venkatpurwar: How hplc column selection according to structure? How mobile phase buffer selection on molecule structure?
792in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
837If 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
856Post New Analytical Chemistry Questions
In performance Check of GC Why Hexadecane Peak is Considered
What is the difference between Discriminating media and DPDM(Dissolution Profile with Different Media)
What is delay volume?
What is the use of tlc and hplc? And when and where use?
iam usig ph buffers merk. manually how to prepare ?
How would you decide dissolution medium for NCE compound of class I drug
i want model written test paper for the post of analyst in IOCL(indian oil corporation ltd) any one pls help me
Why irmoisture balance is used for corrugated box moisture testing
which batch require to use for analytical method validation?
What is the formula to determine the concentration of M of a solution given the % transmittance? Use %T = 43.7 as an example.
we are performed SOR for a particular product the limit is -6 to -10.We face particular bathes it is not meeting the specification.we performed diffrent instrument diffrent analyst we are getting diffrent diffrent results.solvent is dimethyl sulfoxide what could be the reasion
if peak get problamatic then what require to do?
Many times I don't got a caffeine peak in calibration of hplc using guard column ❓
what is mean by covalidation
what is mean by dissolution hydrodynamics?