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If we have 5 strength which is not dose proportinate and excipients also diffrent in each strength then how we can proceed for Force degradation? and excipient are same but not dose propotinate the how FD?
858If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?
1040how decide the clining method and cleaning method validation require for this perticular products?
818Post New Analytical Chemistry Questions
IS THERE ANY EQUIPMENT TO CHECK AND CALCULATE THE POLARITY OF A LIQUID?
why cone formation during dissolution?
Why a1% value is used for some product ? What is the criteria for selection a1% value ?
In rs method development when we are going area normalization method to dilute standard method?
what are the guidelines for analytical method validations?
if rsd failed then what require to do?
Ratio of Water and Acetonitrile(diluent) is not recommended to use in cleaning method validation,why?
What is control room temperature and which guide line says?
How do we get end points and how many end points are possible for citric acid and di-acid not theorotically answer should be given practically.
Which parameter require to do for analytical method equivalency?
how to get accurate result for Residue on evaporation in purified water
What is related substance by HPLC impurity limits as per USP?
how you start the solubility study?
How can the GC or HPLC method is selected to determine the impurity profile in drug product?
in each media we require to use SLS? how to proceed?
