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 5328Why triethylamine and o-phosphoric acid used while setting pH of mobile phase during HPLC Analysis?
6 33604why RID detector is used for selective materials like Mannitol, Hydroxyethyl Starch and Sorbitol?
5 12457For Dissolution test why we are Performing 6 Bowls why not more.any were mentioned or in what basis we are performing? --------Veerabhadrarao.M
2 12136In 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 19439A new drug substance found fail to meet specification for an unknown Impurity during stability study(Specific change),how would further proceed?
2 7342Post New Analytical Chemistry Questions
What is dose dumping? why require to do?
what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
What is the diffrence in japan mkt requirement in analytical method validation over US?
How to know the estimated LOQ concentration in ppm
What is diffrence between extractable volume and deliverable volume? Answer pls
how can give the expiry period and restadardisation of volumetric solution
What is related substance by HPLC impurity limits as per USP?
what is biorelivent dissolution media?
What is the formula to determine the concentration of M of a solution given the % transmittance? Use %T = 43.7 as an example.
If vendor having more imp than monograph then how to proceed? and how to set spec?
can i use hplc detector to uplc and why?
What are the primary considerations in extractables and Leachables ?
how to set sample and standard concentration in RS method?
1.What is the difference between method validation and method verification 2.Which guidelines proposed to method transfer
What is shaking level in GC?