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Answer Posted / vasundhara,vijaya clg
michail tswett in 1906
| Is This Answer Correct ? | 6 Yes | 5 No |
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Which parameter require to do for analytical method equivalency?
in OSD forms require to use gas chromatography?
How to determine water content of bis tetrazole amine mono ammonium salt
before starting analytical method valodation what you checking? and how giving preference to start validation?
what is mean by nitrosamine impurities?
what is mean by ambient temperature?
what is the principle involved in turbidometry and nephelometry ?
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.?
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
if instrument calibration fails then what require to do?
Why we check moisture,ash & AIA in product
how you determine moist.of NaOH sol or NaOH flacks
EXPLAIN THE CALCULATION PART OF AN KF TITRATOR CALIBRATION WITH SUITABLE EXAMPLE
why we use a particular hplc column for a particular compound give reasons?please
What is delay volume?
