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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?
889What is the formula for relative diffrence for standard solution in solution stability in validation?
801[3/30, 13:29] Manoj P Venkatpurwar: How hplc column selection according to structure? How mobile phase buffer selection on molecule structure?
791in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
836If 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
1.What is the difference between method validation and method verification 2.Which guidelines proposed to method transfer
Many times I don't got a caffeine peak in calibration of hplc using guard column ❓
[3/30, 13:29] Manoj P Venkatpurwar: How hplc column selection according to structure? How mobile phase buffer selection on molecule structure?
is it nessesary to do solution stability for 7 days?
how can give the expiry period and restadardisation of volumetric solution
if you get peak in blank then what require to do?
Why dissolution test is not performed in all of the products
How do we quantify crystaline and amarpous forms by using (NMR, XRD)spectroscopic techniques? Which any others instruments are useful for this quantification? explain
for inorganic molecules require to do RS, Assay and disso?
in dissolution why pool sample needed? in which type of drug pool sample need?
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.?
In Dissolution Test why limit is define Q+5% what is the role of +5%.
in which situation require to use paddle and basket?
How much is the standard area for glc analysis
if content uniformity passing but dissolution varrying then what is next step?
