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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?
801If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?
988how decide the clining method and cleaning method validation require for this perticular products?
755Post New Analytical Chemistry Questions
How do we fix the sample concentaryion in hplc method development?
what is mean by ambient temperature?
how to select short coloum and long coloumn for new molecule
Did anybody have method for acetyl cysteine effervescnce tablet
in dissolution why pool sample needed? in which type of drug pool sample need?
WHICH STANDARD WE USE IN SILICA ANALYSIS IN SILICA-GEL METHOD FOR SOLID SAMPLE
Why potassium dichromate is used in calibration of uv?
What is dose dumping? why require to do?
how the compound separate in coulunm,explain
UV and PDA detector, which have less signal to noise ratio?
In which situation we require to analytical method validation of excipient?
how to qualify the impurity?
What is the use of tlc and hplc? And when and where use?
why require to add enzymes in capsules dissolution only? is it require to tablet also?
For limit test of heavy metals in BP, Method C require that the substance is ignited at a temperature not exceeding 800 °C. Why confines such the temperature?
