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  Question  Asked @ Answers Views     select
 
How to set impurity limits for Related substances test.  0  15
Anyone have any idea when to conduct Uniformity of Weight (UOW) and when need to conduct Uniformity of Dosage Units (UOD) or when need both? I read BP it only said if average weight < or = 0.04g then just conduct UOD, no need UOW. Under UOD section, it doesnt say when need to conduct UOD but just said UOD got two type, one is Mass Variation (MV), another is Content Uniformity (CU) and under what conditions to conduct them. For USP, no UOW section, only got UOD section. Hovid-Berhad   0  55
please explain the job responsibilities of quality assurance..  0  63
while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that  0  107
How to register or submit drug master file to any regulatory agency?  2  302
what is the disintegration time of mouth dissolving tablet Unimarck-Pharma  2  390
why we have to use only 900 ml buffer in dissolution apparatus ? what are the conditions that favours the selection of volume of buffer?  1  403
what is the mechanism of action of local anaesthetics?  0  149
What is the different between GMP & cGMP ?  1  428
What are the significance of MKT in stability study. Alembic  1  871
Which types of deviations are followed in pharmaceuial API manufacturing industry? Laurus  0  536
What is the differance Between Calibration & Validation MSN-Pharma  5  1397
when i come in contact with any metal items or clothes of fur i find myself shock and when run my fingers on fur clothes or matters, i find sparks. Is there any vitiams deffecieny in my body. If so, what i have to do?  0  266
WHAT IS MEANING OF DEAIATION WITH EXAMPLE  0  241
What are the regulatory commitments in markets like USA, Canada, Europe, Brazil, South Africa and Japan  0  277
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Un-Answered Questions
 
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What was your most difficult experience with this population and how did you deal with it? 319  
Which types of deviations are followed in pharmaceuial API manufacturing industry? 536 Laurus
why didn't you go back to previous employer after shifting to bangalore? 333  
what is meant by artwork review and handling procedure with an example? 270  
Give an example of how you've handled a problem patient. 355  
while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that 107  
What experience do you have in training? 324  
What are the regulatory commitments in markets like USA, Canada, Europe, Brazil, South Africa and Japan 277  
If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can u proceed calibration? 619 Cipla
How to set impurity limits for Related substances test. 15  
Iam a B.PHARMA GRADUATE from DELHI UNIVERSITY and I am looking forward for DRUG INSPECTOR EXAM..kindly mail me any ques papaers reg the same... 280  
How are you qualified for the position of Assistant Clinical Director? 435  
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