Answer / hariram

it is a condition at which the concentration of drug is
maintain in blood after administration of drug due to
continuous flow of blood

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0 Answers  

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What is sink condition, how far it is maintaining in the dissolution?

2 Answers   Reddy Labs,

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What is the difference between Calibration & Validation?

2 Answers  

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What is difference between method validation and method verification?

1 Answers  

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what is Alcova

2 Answers   Ajanta Pharma,

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How to determine peak purity index in Empower software? What is the acceptance criteria of peak purity index to consider the peak purity is pass?

0 Answers   Kemwell,

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Why and when RRF is required to be known in RS Method? How is it helpful during method development?

3 Answers   Panacea,

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i have finished my B. Pharm ,i want to join Pharmacy concil of india, what to do, please suggest me , how to make carrier best in this field, donot wanna go for M. Pharma. please help me.

2 Answers  

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If we get 100% assay of an Initial sample ,and the stability studies of the same sample got 90% dissolution result, and when the same stability sample was analyzed for RS studies no impurities was found . Where the 10% Active substance were gone during dissolution analysis.Please help me in getting the conclusion.

1 Answers   Cipla,

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What is the disintegration time of coated tablets?

3 Answers  

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What is the process validation?

1 Answers  

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What is the difference between uniformity of content and content uniformity as official test for all tablets?

0 Answers  

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