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 Categories >> Sciences >> Health Pharma >> Health Pharma AllOther
 
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Question Asked @ Answers Views     Select
What r the different sop in or plant    0  82
Difference between Change control and Deviation please give the answer elaborately    0  78
what is the leak test procedure of filled bottles (liquid)    0  129
What is difrance between 0. 1 & 0. 10    0  92
Why 3 validation ¬†batches charge in stability ?is there any specific reason for 3 ?    1  260
difference between related substances and purity?    0  535
difference between RF and correction factor?    0  540
how many deviation allowed    0  547
from hplc chromatogram how can we say that calibration is needed now?    0  733
diffrence between known impurity and specified impurity?    2  930
Tolerance limit for dissolution media rpm sampling point.    0  902
using of chemical standards in HPLC he customer gave 100.2% what potency i will use this potency in hplc? vivimed-labs   0  940
How to set impurity limits for Related substances test.    1  856
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  880
please explain the job responsibilities of quality assurance..    0  600
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If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can u proceed calibration? 1357
why didn't you go back to previous employer after shifting to bangalore? 520
What r the different sop in or plant 82
Tell us about a time when you failed to meet a deadline. What were the repercussions? 750
please e-mail me the model of Tamil Nadu drug inspector question papers 921
Difference between Change control and Deviation please give the answer elaborately 78
What is the basic requirement for preparing drug master file , like EDMF , USDMF ? 1046
Tolerance limit for dissolution media rpm sampling point. 902
what is meant by artwork review and handling procedure with an example? 469
How can I assign a retest date for solvents e.g. toluene, methanol, etc? 776
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... 478
Tell us about your oncology experience. 745
What experience do you have in training? 534
when we connect the capacitor banks in series with the circuit? 2 144 pH is having unit? 564
difference between RF and correction factor? 540
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