Answer Posted / irshad mansoori

i would also like to favor of this answer, but if u have
work experience related to that sector, then please
elaborate it, because it will be helpful to you, as well as
for the company to give you most priority rather than fresher.

how impurity is analyzed in a tablet

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What are the limits for LOD and LOQ?

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What is the difference between Analytical method validation and Analytical method transfer?

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i am preparing for Drug inspector exam.If u have previous questions please send me.

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if calibration of 12 bowl dissolution apparatus does not meet a single stage procedure how you can proceed calibration

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1.why did you choose this career 2.what is pharmacists ideal job

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principle of dissolution

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How we define validity of any Reagent , Indicator and Volumetric Solutions

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what is the calculation for getting the tablet weight and the punch size, Eg..if there is a 8/32 punch then how to measure tablet weight????

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What is the difference between temporary change control and deviation?

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What is validation, validation protocol and validation master plan?

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how to make Enrofloxacin 20% solution & whats remedy to avoid crystal formation in this batch after 15 -20days? Please anybody assist in it

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what is purpose of slow,medium,fast sampling in process validation ?

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HI, I srinivas , was shortlisted for interview of Ph.D. PROGRAMMES FOR ACADEMIC SESSION 2012, I have interview on 17-nov-2011. Sir can you tell me about interview, how to prepare for it. How it will be? It's my first interview sir, i don't know how to face it. Kindly help me sir, Thanking yoU,

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how you can fix the known and unknown impurity limit for any drug substance

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