If we do accuracy at same concentration at which linearity planned,what is the need to do linearity separately?

2282

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?

788

in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?

806

How we choose the mobile phase for method development.?

1199

WHY pKa value is more important than pH value of the mobile phase in HPLC?

1750

WHAT IS THE USE OF STARTER ?????????

2397

if tech transfer fails whay require to do?

823

What is the Formula for coreletion coefficient in plhplc calibration

1806

What if impurity area in control sample coming more as compared to LOQ level of impurity ?

1586

what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?

880

how can I make the copper get white bye any salt or acit?

2194

how to selecet an exact coloumn for an new molecule development by hplc how to select exact salt as buffer for new molecule development by hplc what is the the process to select the mode of saparation of compoundes by hplc what is the use of ph of buffer what is use of buffer,ph,organic phase,ans methods how the molecules get saparated in coloumn,

2581

for heavy metal test lead used in which form pure form or any other form for preparation of lead standard sol

6047

How we can identify process related and degradation impurity in single method with short period?

795

what is %labelled amount in content uniformity of dosage unit and its calculation?

5198