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.?
675what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
856What is the formula for relative diffrence for standard solution in solution stability in validation?
755[3/30, 13:29] Manoj P Venkatpurwar: How hplc column selection according to structure? How mobile phase buffer selection on molecule structure?
718in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
785If 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
813Post New Analytical Chemistry Questions
A ha tc is actual defination of retention time?
in dissolution why pool sample needed? in which type of drug pool sample need?
Why we use potassium dichromate in uv calibration Exact reason behind it??
1)What's the meaning of Absorption,give a example. 2)What's the meaning of Adsorption,give a example. 2)what is the difference between Absorption and Adsorption.
in each media we require to use SLS? how to proceed?
What is the requirement for brazil in the analytical method vslidation comparr to ich?
why sre you used Potassium hydrogen phthalate in standarisation of 1N NaOH and 0.1 N Perchloric Acid?
How to choose the which salt is suitable for mobilephase
how many types of balance calibration test?
about method developement in hplc
why salisylic acid not using now days for disdolution calibration?
UV and PDA detector, which have less signal to noise ratio?
Please give idea about method development for cleaning method and how maco level establish
How to know the estimated LOQ concentration in ppm
how to set sample and standard concentration in RS method?