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

why we are using in ph calibrations ph4,7,9.2 buffers only?

5 Answers   Reddy Labs,

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7 Answers   GVK,

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what buffer you can select for acidic nature analyte and how ?

2 Answers   Dr Reddys,

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0 Answers   GHI, Siemens,

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2 Answers   Celon Labs, Laurus,

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why required specificity in valdation

3 Answers  

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1 Answers   Pfizer,

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reasons for negative peaks in chromatography

5 Answers   DRL,

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2 Answers  

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In the isomers,enantiomers give the only physical properties present such that no chemical properties present.

0 Answers   Laurus,

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What is the procedure for investigation of an OOS (Out of specification) results?

4 Answers   Biocon, Dr Reddys, Reddy Labs,

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