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What is the accrptance criteria in RSD for RS method precision on basis of impurity percentages?
785How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?
704if your product is soluble in 0.1n hcl and water then which you choose as media from these 2 media?
653in dissolution if one bowl got 70 percent 2nd bowl got 80 percent and 3rd bowl got 90 percent then how proceed?
731Post New Analytical Chemistry Questions
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?
what is %labelled amount in content uniformity of dosage unit and its calculation?
what is mean by nitrosamine impurities?
Please give idea about method development for cleaning method and how maco level establish
what is the principle of UV Vis spectroscopy, AAS, ICP OES,ICPAES, ICP-MS and FTIR
How to start the dissolution development for unknown tab?
What should be the level/ Percentage of Arsenic in Arsenic free zinc.
Home heating oil or furnace oil what is made from? Can (base oil plus diesel/kerosen) = home heating oil?
what is the origin to prepare standard operating procedure
why require the ph, buffer during hplc mobile phase?
Hi sir if any product monograph not given known impurities (may be 5 impurities) specifications then how we require to proceed for inhouse formulation?
[3/28, 20:52] Manoj P Venkatpurwar: how many impurities require to inject in assay specificity that how we can find out? and in Rs also how?
can we use the same detector in HPLC as well GC and what could be the differences we can find in the final chromato graph in any aspects?
what are the guidelines for analytical method validations?
can i use hplc detector to uplc and why?
