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if content uniformity passing but dissolution varrying then what is next step?
How would you decide dissolution medium for NCE compound of class I drug
which batch require to use for analytical method validation?
Why are use silicon oil mr?
what is difference in ods I ods II is this is realy from sorbent / packing characteristics or from other means
How we can identify process related and degradation impurity in single method with short period?
HI,I CLEARED BOB CLERK EXAM. MY INTERVIEW WILL BE ON 9TH OCTOBER,2010.PLEASE SEND ME INTERVIEW QUESTIONS AND ANSWERS. THANK YOU.
How can the GC or HPLC method is selected to determine the impurity profile in drug product?
sop of a uv visible spectrophotometer double beam elico model
process of Diclofenac sodium,IP.
function of detecter in hplc ,gc and spectroscopy? function of carrier gas in gc?
How can we calculate "confidence interval" in analytical method validation? Pl. explain with example.
In GC calibration,what is the procedure to calibrate the TCD (thermal counductivity detector)suggest ?
if your product is soluble in 0.1n hcl and water then which you choose as media from these 2 media?
Why only hydroxy naphthol blue indicator is used for standardisation of 0.05M EDTA solution instead of solochrome Black T or Euriochrome Black T indicator which is used for all sample analysis with 0.05M EDTA solution?
