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In pharmacopeal solibility parameter of a material, is et essential to test all paramete? If 70-75% parameter passes can we assess that the material is satisfactory or not?
1 5391Why triethylamine and o-phosphoric acid used while setting pH of mobile phase during HPLC Analysis?
6 33860why RID detector is used for selective materials like Mannitol, Hydroxyethyl Starch and Sorbitol?
5 12649For Dissolution test why we are Performing 6 Bowls why not more.any were mentioned or in what basis we are performing? --------Veerabhadrarao.M
2 12259In Number of Theoretical Plates (N) = 16 (tr/w)2. where tr: retention time, and W: peak width. My Question is here in formula what is 16.Can u explain briefly? ---Veerabhadrarao.M
3 19614A new drug substance found fail to meet specification for an unknown Impurity during stability study(Specific change),how would further proceed?
2 7443Post New Analytical Chemistry Questions
how to set sample and standard concentration in RS method?
What if impurity area in control sample coming more as compared to LOQ level of impurity ?
How to choose the which salt is suitable for mobilephase
how you start the solubility study?
can we use the same detector in HPLC as well GC and what could be the differences we can find in the final chromato graph in any aspects?
how will you do the prep for unstable componds?
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 separately
What is related substance by HPLC impurity limits as per USP?
How require to perform linearity as per ANVISA? What are the acceptance criteria?
what is the disso medium for tropsiun chloride
How you develop a method in HPLC?
WHICH STANDARD WE USE IN SILICA ANALYSIS IN SILICA-GEL METHOD FOR SOLID SAMPLE
cefoperozone and sulbactam inj. hplc test method
why lactose has less charges when packed in steel containers when compared with packing of lactose in polyamide material?
USP methodology, EP methodology, IP methodology, among three if possible to use one methodology for qualify working standard to use USP, EP, IP ? Please explain...
