One pH means how much volts and milivolts?
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what are risk assement in the analytical qbd?
In HPLC (Waters) software Empower1,2 &3 what is the updation for each version
give clarity of linearity and range in method validation
what is the procedure for cleaning of lenses of hatr accesory of ftir instrument?
Related substance method equivalency on control sample or spiked sample?
How can the GC or HPLC method is selected to determine the impurity profile in drug product?
how many types of balance calibration test?
Please tell me about the pH of Polycaboxylic ether is it in the 5-6 range ever or more than 6
If change in specification which parameter require to do for validation? if change in chromtographic condition then which parameter? if api change then which parameter? if change composition then which parameter? if old method not work out then whicj parameter? if additional one impurity added then which parameter of validation require to do on above each conditions? elaborate separately
How to compare XRD graphs against standard and carry polymorpism study of API's by powder XRD method?
How we can identify process related and degradation impurity in single method with short period?
what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
What is the difference between purge septum flow and column flow in gas chromatography?
Why irmoisture balance is used for corrugated box moisture testing
before starting analytical method valodation what you checking? and how giving preference to start validation?
