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

What is the definition of water content or moisture content,what is the procedure going on w.c amalysis?

1 Answers   Cipla, KIYI,

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wat is reverse phase in hplc

2 Answers  

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in determination of(acetone) moister content we are using methanol replaced by pyredine.what hapend in that reaction.

2 Answers   Glenmark, Neuland,

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what is difference between drug products and drug substance?

5 Answers   DRL,

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what is the difference between capillary and glass column in GC

1 Answers  

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Wath is the differenc between two column HPLC wich have the samme support , lenth , pore size, etc.. But different name .for exemple : Spherisorb / lichrosorb

2 Answers   NDA,

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Why are using in Hi,zero air, Ni gass are used GC

5 Answers   Aurobindo, ELBS, Vimta Labs,

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how decide the clining method and cleaning method validation require for this perticular products?

0 Answers  

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identification is for unknown? qualification for known? reporting for LOQ?

0 Answers  

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What is the definition of RRF

2 Answers  

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why cone formation during dissolution?

0 Answers  

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1.What is the difference between method validation and method verification 2.Which guidelines proposed to method transfer

0 Answers   Granules,

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