Answer / suresh naidu

Q is the specification limit( the mean of individual tablets tested should be not less than Q) of the dissolution test.

Q+5 is the criteria for which the dissolution passing with 6 tablets at S-1 stage (optimum release).:

What is limit of cleaning validation?

0 Answers  

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In dissolution test why sample is withdrawn from top of the paddle and not less than 1 cm away from wall?

0 Answers  

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why we use sodium salicylate for UV chamber calibration?

1 Answers   Hetero, SGS,

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what is the principle of AWC (Auto weight control) in compression machine.

10 Answers   Apotex, Cipla, Dr Reddys, Glenmark, Hetero, Lupin, MSN, Reddy Labs, Unichem,

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Hi, I am studying Bpharmacy final year. 1)I want to interview questions for facing basic interview.please help me to provide model papers for all pharma companies and give ur valuable suggestions also. 2)Send me important links for BPharmacy interviews. 3)How should i prepare for facing interview,please give me suggestion. My email id:1010.murthy@gmail.com

0 Answers   Abbott, Cipla, Ranbaxy,

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how many types of deviations? describe

3 Answers  

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1.why did you choose this career 2.what is pharmacists ideal job

0 Answers   Wockhardt,

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Why we use the placebo in analysis?

2 Answers  

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what is the exact diff betwen the uniformity of weight & uniformity of content?

3 Answers   Lupin,

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What types of columns are used in GC?

1 Answers  

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Please send me the model papers of Drug Inspector

1 Answers   Phamatech,

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How we fix the validity period of a Normal solution and re-standardization due date

2 Answers  

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