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Answer Posted / t reddy
quality control is a set of procedures to check whether the drug products is achieving the customers needs or not.....
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if your impurity coeluting with each other in that situation how require to set specification? is it acceptable?
Ph meter can show more than 14 ph reading? Why ph range in between 1 to 14 only?
how you fix the limits of impurities?
In HPLC Calibration, On which basis RSD Limit of noise test is fixed (NMT 33.0 % )
From where require to take the RLD sample?
How do we fix the sample concentaryion in hplc method development. What is the basis?
For titration in anhydrous media with perchloric acide, if lack of titrator, Which indicator is been used for replacement. How calculate pH of test solution to choose suitable indicator?
how many types of balance calibration test?
What is similarity factor?
in gas chromatography what is the difference between gas flow rate and average linear velocity ?
in each media we require to use SLS? how to proceed?
We use hicrome 10 cxs column in hplc analysis....pls tell me.. what is the meaning of 10 cxs?
What is the diference between residual solvents and organic volatile matter
Tell me something about Vitamin A test method by HPLC
How can the GC or HPLC method is selected to determine the impurity profile in drug product?
