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how will you do the prep for unstable componds?
Why to use propyl paraben in HPLC gradient calibration
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
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?
Why potassium dichromate is used in calibration of uv?
WHY given much noise PDA dector then VWD Dector
Why dissolution test is not performed in all of the products
in which situation require to take incident in validation?
How we can identify process related and degradation impurity in single method with short period?
can i use hplc detector to uplc and why?
Hi sir if any product monograph not given known impurities (may be 5 impurities) specifications then how we require to proceed for inhouse formulation?
what are the standard methods for HPLC?
What is delay volume?
How do we fix the sample concentaryion in hplc method development. What is the basis?
How we performed the force degradation for drug substance, is any specific guideline is available for each parameter(Acidic, basic, oxidation,heat)? what conditions you mentained for above parameters.
