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...
1544is it necessary to do HPLC calibration at wavelength 315nm if we are doing analysis at this wavelangth
1648we are performed SOR for a particular product the limit is -6 to -10.We face particular bathes it is not meeting the specification.we performed diffrent instrument diffrent analyst we are getting diffrent diffrent results.solvent is dimethyl sulfoxide what could be the reasion
1346Post New Analytical Chemistry Questions
why require to add enzymes in capsules dissolution only? is it require to tablet also?
Difference between hlaf and rlaf
what is the disso medium for tropsiun chloride
How do we fix the sample concentaryion in hplc method development?
In HPLC Calibration, On which basis RSD Limit of noise test is fixed (NMT 33.0 % )
If vendor having more imp than monograph then how to proceed? and how to set spec?
how can give the expiry period and restadardisation of volumetric solution
How you develop a method in HPLC?
what is mean by 40 in the dissolution basket mesh size?
What is Band broading effect explain
effect of pore size, pore volume, partical size, column length, carbon load on retention time? what is carbon load? what is the use?
What is stray light in uv what are units for stray light
from where i get mortar pastle for glass bottle crush? it's required for testing of it?
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.?
in stress study if your api not soluble in hcl naoh h2o2 then what require to do?
