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  Question  Asked @ Answers Views     select
 
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  51
please explain the job responsibilities of quality assurance..  0  55
while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that  0  100
How to register or submit drug master file to any regulatory agency?  2  289
what is the disintegration time of mouth dissolving tablet Unimarck-Pharma  2  376
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  390
what is the mechanism of action of local anaesthetics?  0  146
What is the different between GMP & cGMP ?  1  411
What are the significance of MKT in stability study. Alembic  1  853
Which types of deviations are followed in pharmaceuial API manufacturing industry? Laurus  0  525
What is the differance Between Calibration & Validation MSN-Pharma  5  1371
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  260
WHAT IS MEANING OF DEAIATION WITH EXAMPLE  0  233
What are the regulatory commitments in markets like USA, Canada, Europe, Brazil, South Africa and Japan  0  271
What are the filing requirements for ANDA-USA, Europe, Brazil, South Africa, Japan and Emerging Markets  0  831
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Un-Answered Questions
 
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while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that 100  
Which types of deviations are followed in pharmaceuial API manufacturing industry? 525 Laurus
why you are become a medical representative 278  
Give an example of how you've handled a problem patient. 353  
If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can u proceed calibration? 610 Cipla
What are the filing requirements for ANDA-USA, Europe, Brazil, South Africa, Japan and Emerging Markets 831  
What experience do you have in training? 322  
You will be required to interact with patients. Tell us about your previous experience with patients and how did you deal with the experience. 375  
What are the regulatory commitments in markets like USA, Canada, Europe, Brazil, South Africa and Japan 271  
what is the test scenario? 271 UHG
please explain the job responsibilities of quality assurance.. 55  
How should the Medical Librarian interact with training staff? 383  
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