Answer Posted / priyanka
no.of equivalent wt. dissolve in 1litr of solvent
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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.?
why require to do water content for drug product?
AT WHAT CONDITIONS WILL YOU ANALYSE A SAMPLE,WHICH ARE PRESERVED AT OTHER THAN THE AMBIENT CONDITIONS?(ie COLD STORAGE SAMPLES BELOW 20* CENTIGRADE?
what parameters we will consider while developing a HPLC method and how we confirm our HPLC method is valid?
How we can identify process related and degradation impurity in single method with short period?
Basic principle of ESI?
What is rs test why we are performing rs test?
if rsd failed then what require to do?
WHY given much noise PDA dector then VWD Dector
In HPLC Calibration, On which basis RSD Limit of noise test is fixed (NMT 33.0 % )
How can the GC or HPLC method is selected to determine the impurity profile in drug product?
if instrument calibration fails then what require to do?
How doing qbd practically?
which situation gc hs and gc als require to use?
How to set analyticl specification for combination products?
