Answer / kanakadurga

Cleaning validation for is the methodology used to assure
that a cleaning process removes residues of the active
pharmaceutical ingredients of the product manufactured in a
piece of equipment, the cleaning aids utilized in the
cleaning process and the microbialattributes. All residues
are removed to predetermined levels to ensure the quality of
the next product manufactured is not compromised by waste
from the previous product

IS THERE ANY EQUIPMENT TO CHECK AND CALCULATE THE POLARITY OF A LIQUID?

0 Answers   Reddy Labs,

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Why we use uracil and caffeine in hplc calibration

6 Answers   Alchem, Reddy Labs,

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why reference flow required during hplc analysis on rid?

1 Answers  

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in dissolution in one tablets two molecule one is losartan & second is HCTZ losartam is complies in s1 stage & hctz is complies in s2 stage then how to report result losartan s1 stage result or losartan s2 stage result

1 Answers   Dishman,

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what is the definition of Precision.

4 Answers   Cipla,

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What is viod volume and peak purity in HPLC?

0 Answers  

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What is excipient in drug product?

1 Answers   Lupin,

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difference between calibration and validation

2 Answers   Mylan,

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Explain the relations between number of carbon atoms in alkanes and retention time ?

0 Answers   College School Exams Tests,

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In Number of Theoretical Plates (N) = 16 (tr/w)2. where tr: retention time, and W: peak width. My Question is here in formula what is 16.Can u explain briefly? ---Veerabhadrarao.M

3 Answers   Micro Labs, Richter Themis, Sun Pharma,

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If compound Pka is 5 then which buffer you will select ?

5 Answers   Avra, GVK,

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In Force degradation Study Compound is not degrade in any condition , also in higher stress what can i do ?

4 Answers   Alembic,

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