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.?
281what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
334What is the formula for relative diffrence for standard solution in solution stability in validation?
299[3/30, 13:29] Manoj P Venkatpurwar: How hplc column selection according to structure? How mobile phase buffer selection on molecule structure?
300in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
341If 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
349Post New Analytical Chemistry Questions
How to know the estimated LOQ concentration in ppm
in which situation ion pair require to use?
What is column in chromatography?
How doing qbd practically?
what is mean by peak intigrity?
In Assy by potentio metry titration method how select MET U ,DET U, SET U,
Which are the diffrent grades of api in pharma?
How to calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample
how to qualify the impurity?
Is it nessesary all multimedia dissolution require descriminatory?
What is Band broading effect explain
Why only 1.2 million lux hours require in photostability study?
If vendor having more imp than monograph then how to proceed? and how to set spec?
What is stray light in uv what are units for stray light
if content uniformity passing but dissolution varrying then what is next step?