Answer / kishor solanke (alkem)

Protocol shall be prapared for to establish the
restandardisation date foe the volumetric solution. Date
shall be fixed on the basis of standaradisation study of
volumetric solution on fixed or predifined in protoal
interval, e.g. 1,2,3,7,15 days etc intervals. The % RSD
shall be NMT 0.2% at all intervals.

How related substance method is developed for new compound which is not official in the pharmacopeia?

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In dissolution test why sample is withdrawn from top of the paddle and not less than 1 cm away from wall?

1 Answers   Glenmark,

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ONLINE TRAINING IN ORACLE CLINICAL 4.6 (Clinical Data Management) and SAS -SDTM mapping

1 Answers  

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what is the major definition and difference between uniformity of content and content uniformity as official test for all tablets?

4 Answers   Wockhardt,

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What is the difference between Calibration & Validation?

2 Answers  

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if calibration of 12 bowl of dissolution apparatus does not meet a single stage how you can proceed calibration

1 Answers  

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what is mean by stability study?

4 Answers   BioPlus,

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In Stability testing if significant change occur then what is the action plan?

4 Answers   Bliss GVS Pharma, MSN Pharma,

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What do you mean by CAPA?

2 Answers  

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If granules are over lubricated what defect arises in tablet compression how we solve this problem.

0 Answers   BioPlus, Inventia Healthcare,

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How can you fix the known and unknown impurity limit for any drug substance?

0 Answers  

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Hai,i had completed my M.pharmacy.i want the coaching centres for drug inspector exam at hyderabad,pls help me nd wen wil b the DI exam conducted in 2012 mostly,pls also forward the model papers.. pls reply me at vislawath.jyothi@gmail.com

0 Answers   Akums,

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