what is the defination of calibration & verification?
Answer Posted / basha
calibraion is the checking the instrument with reference
standards they are in limit or out of limit
| Is This Answer Correct ? | 5 Yes | 2 No |
Post New Answer View All Answers
What is viod volume and peak purity in HPLC?
What is the principle of HPLC, GC, LCMS, GCMS,LC QQQ, GC QQQ, LC Q TOF and GC Q TOF. What are the applications and Specificity?
WHY pKa value is more important than pH value of the mobile phase in HPLC?
In performance Check of GC Why Hexadecane Peak is ConsideredÂ
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?
In IR spectra, generally a molecule vibrates without apply emr or ir light?
Why sodium hydroxide used for maintain pH of phosphate buffer
why require the ph, buffer during hplc mobile phase?
What is diffrence between extractable volume and deliverable volume? Answer pls
inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?
please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development
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 would you decide dissolution medium for NCE compound of class I drug
What is the main difference between ODS1 and ODS2 Hplc column.
what parameters we will consider while developing a HPLC method and how we confirm our HPLC method is valid?