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.?9
what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?23
What is the formula for relative diffrence for standard solution in solution stability in validation?17
[3/30, 13:29] Manoj P Venkatpurwar: How hplc column selection according to structure? How mobile phase buffer selection on molecule structure?15
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?10
If 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 separately13
From where require to take the RLD sample?
in which situation ion pair require to use?
how require to interprit the method precision data of hptlc?
Which are the diffrent grades of api in pharma?
what is third integration
How can I develope method of dissolution by HPLC OR UV
Why use only methanol,used determinationof moisture content not use other solvents
why we are using benzene, anyline in acetic anhdride assay titration method?
what is procedure of actual procedure for registration of drug?
what is the origin to prepare standard operating procedure
Tell me about analytical method validation in QC
What is column in chromatography?
WHAT IS THE USE OF STARTER ?????????
how much mass should be there in volumetric flask while in preparation of sample for assay?