Why dissolution test apparatus calibration with salycilic acid tablets was stopped by FDA&USP from the year of 2009?
1 8089Post New Analytical Chemistry Questions
what is classification of elemental impurities? what is risk assement in elemental impurities?
how can give the expiry period and restadardisation of volumetric solution
why require to do water content for drug product?
from where i get mortar pastle for glass bottle crush? it's required for testing of it?
how you determine moist.of NaOH sol or NaOH flacks
Please tell me about the pH of Polycaboxylic ether is it in the 5-6 range ever or more than 6
EXPLAIN THE CALCULATION PART OF AN KF TITRATOR CALIBRATION WITH SUITABLE EXAMPLE
In Dissolution Test why limit is define Q+5% what is the role of +5%.
why we should take dst factor for below 1%moisture samples
in dissolution if one bowl got 70 percent 2nd bowl got 80 percent and 3rd bowl got 90 percent then how proceed?
In HPLC Calibration, On which basis RSD Limit of noise test is fixed (NMT 33.0 % )
How to compare XRD graphs against standard and carry polymorpism study of API's by powder XRD method?
While performing TOC sst analysis Zero shift disabled & sample analysis zero shift enabled why?
why we use glass fiber filters use in some situation?
How we can identify process related and degradation impurity in single method with short period?