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Answer Posted / sivasakthi
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What is mean by PDR?
how will you do the prep for unstable componds?
what is mean by nitrosamine impurities?
What is the use of tlc and hplc? And when and where use?
In which situation we require to prepare the standard solution from sample in Related substance method?
what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development
What is rs test why we are performing rs test?
What is the principle of Thermal conductivity detector and FID?
what is %labelled amount in content uniformity of dosage unit and its calculation?
if your product is soluble in 0.1n hcl and water then which you choose as media from these 2 media?
How to determine water content of bis tetrazole amine mono ammonium salt
How to set analytical specification for combination products?
in which situation ion pair require to use?
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?
