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 Categories >> Sciences >> Health Pharma >> Health Pharma AllOther
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Question Asked @ Answers Views     Select
Tolerance limit for dissolution media rpm sampling point.    0  10
using of chemical standards in HPLC he customer gave 100.2% what potency i will use this potency in hplc? vivimed-labs   0  24
How to set impurity limits for Related substances test.    0  38
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  76
please explain the job responsibilities of quality assurance..    0  79
while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that    0  121
How to register or submit drug master file to any regulatory agency?    2  337
what is the disintegration time of mouth dissolving tablet unimarck-pharma   2  426
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  433
what is the mechanism of action of local anaesthetics?    0  164
What is the different between GMP & cGMP ?    1  459
What are the significance of MKT in stability study. alembic   1  906
Which types of deviations are followed in pharmaceuial API manufacturing industry? laurus   0  554
What is the differance Between Calibration & Validation msn-pharma   6  1457
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  277
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Un-Answered Questions
 Question Views   Select
What is the basic requirement for preparing drug master file , like EDMF , USDMF ? 511
using of chemical standards in HPLC he customer gave 100.2% what potency i will use this potency in hplc? 24
please explain the job responsibilities of quality assurance.. 79
What was your most difficult experience with this population and how did you deal with it? 323
plz.mail me model papers of drug inspector of chhattisgarh..or MP.if Posible. Mail, 566
what is the test scenario? 278
what is meant by artwork review and handling procedure with an example? 273
when we connect the capacitor banks in series with the circuit? 2 144 pH is having unit? 298
concomitant administration of 6-mercaptopurine and which product results in severe bonemarrow suppression? 445
What are the regulatory commitments in markets like USA, Canada, Europe, Brazil, South Africa and Japan 285
If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can u proceed calibration? 631
Do you think it is possible to rehabilitate? 355
why an employee go for medical representative instead of quality? 261
How are you qualified for the position of Assistant Clinical Director? 445
how many clauses are there in iso? give me the clauses details? 550
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