Answer Posted / ragav

Validation in the pharmaceutical and medical device
industry is defined as the documented act of demonstrating
that a procedure, process, and activity will consistently
lead to the expected results.
Making measurements with any analytical method or
instrument requires calibration to ensure the accuracy of
the measurement. There are two common calibration
procedures: using a working curve, and the standard-
addition method. Both of these methods require one or more
standards of known composition to calibrate the
measurement.

pharma industries oriented

2255

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if you have given a blank water how you analyse by general analytical techniques?

2036

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WHAT IS THE PURPOSE WE USE HCL, CHOPPER, BURNER, MONOCHROMATOR in AAS? PLEASE EXPLAIN BRIEFLY

2622

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Why dissolution test is not performed in all of the products

2539

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if you get peak in blank then what require to do?

981

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Why we used in n-butyl acetate water content terminology while in ethyl acetate we used moisture content terminology?

1866

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HI,I CLEARED BOB CLERK EXAM. MY INTERVIEW WILL BE ON 9TH OCTOBER,2010.PLEASE SEND ME INTERVIEW QUESTIONS AND ANSWERS. THANK YOU.

2253

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from where i get mortar pastle for glass bottle crush? it's required for testing of it?

2271

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Which parameter require to do for analytical method equivalency?

788

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if content uniformity passing but dissolution varrying then what is next step?

886

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How to decide assay range for non pharmacopeial API analysis by HPLC? Could you give me any reference for same e.g Guidelines or Paper publications?

3367

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Why only 1.2 million lux hours require in photostability study?

1046

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what is diffrence between specificity and selecivity?

795

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in dissolution if one bowl got 70 percent 2nd bowl got 80 percent and 3rd bowl got 90 percent then how proceed?

760

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In GC calibration,what is the procedure to calibrate the TCD (thermal counductivity detector)suggest ?

3184

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