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?
760If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?
933how decide the clining method and cleaning method validation require for this perticular products?
705Post New Analytical Chemistry Questions
how you determine moist.of NaOH sol or NaOH flacks
HI,I CLEARED BOB CLERK EXAM. MY INTERVIEW WILL BE ON 9TH OCTOBER,2010.PLEASE SEND ME INTERVIEW QUESTIONS AND ANSWERS. THANK YOU.
if you have given one product then how you determine the impurity in that?
In which situation we require to prepare the standard solution from sample in Related substance method?
in api coa contains only process impurities and in product coa contains degradation impurities?
EXPLAIN THE CALCULATION PART OF AN KF TITRATOR CALIBRATION WITH SUITABLE EXAMPLE
why lactose has less charges when packed in steel containers when compared with packing of lactose in polyamide material?
WHY given much noise PDA dector then VWD Dector
mode of absorption in alimentary canal?
how you fix the limits of impurities?
on the basis of bcs class how to proceed the solubility?
why multimedia dissolution require to do?
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?
What is related substance by HPLC impurity limits as per USP?
Why we select scan range from higer wavelength to lower wavelength in uv visible spectroscopy and ftir spectroscopy ? .