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).:

1.Which drugs are suitable for extended-release formulations? 2.Criteria for selection of drugs for sustained release formulation?

2 Answers   Arges Pharma Biotech,

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What is the relative response factor in related substances?

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maxmimum absorbance of uv spectrophotometer

5 Answers   Cadila,

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0 Answers   Indoco,

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HOW TO PERFORM SATURATION SOLUBILITY IN DISSOLUTION METHOD DEVELOPMENT?

0 Answers   Micro Labs,

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how can u calculate the percentage CDR?

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1 Answers   Habsons,

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In dissolution test why sample is withdrawn from top of the paddle and not less than 1 cm away from wall?

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i had completed my degree with 72% but i dont have good score in gre and tofel and i got an admission into a college in usa is trheir will be any problem if i appear for visa regection because of gre and tofel and i am from science background i lost touch in those subjects.

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what is difference between polarimeter lamp and IR lamp

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