What is the accrptance criteria in RSD for RS method precision on basis of impurity percentages?
305How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?
272if your product is soluble in 0.1n hcl and water then which you choose as media from these 2 media?
274in dissolution if one bowl got 70 percent 2nd bowl got 80 percent and 3rd bowl got 90 percent then how proceed?
328Post New Analytical Chemistry Questions
What is dose dumping? why require to do?
How to determine water content of bis tetrazole amine mono ammonium salt
cefoperozone and sulbactam inj. hplc test method
How we performed the force degradation for drug substance, is any specific guideline is available for each parameter(Acidic, basic, oxidation,heat)? what conditions you mentained for above parameters.
Describe your field experience sample type collected,sample techniques,field measurements taken and equipment used?
Why we select scan range from higer wavelength to lower wavelength in uv visible spectroscopy and ftir spectroscopy ? .
Why a1% value is used for some product ? What is the criteria for selection a1% value ?
why sre you used Potassium hydrogen phthalate in standarisation of 1N NaOH and 0.1 N Perchloric Acid?
what is partion and column chromatography
why glutent are detected in the rice cereal baby food product even manufacturer claimed that they are using rice and milk only?we have using ELISA to do the test,and rice supposed not containing any glutent,rite?We already repeat the test so many times and it still detected.just wondering where the glutent came from?
how to selecet an exact coloumn for an new molecule development by hplc how to select exact salt as buffer for new molecule development by hplc what is the the process to select the mode of saparation of compoundes by hplc what is the use of ph of buffer what is use of buffer,ph,organic phase,ans methods how the molecules get saparated in coloumn,
analytical method validation require to with respect to release specification or shelf life specification?
4. Describe the operation of the Craig apparatus. Chapter.3 Equilibrium Processes in Separations
How do we fix the sample concentaryion in hplc method development. What is the basis?
How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?