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 Categories >> Sciences >> Health Pharma
 
  Pharmacy (280)   Lab Technicians (75)   Health Pharma AllOther (88)
 
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Question Asked @ Answers Views     Select
1.Which drugs are suitable for extended-release formulations? 2.Criteria for selection of drugs for sustained release formulation?    0  9
what are the GLP activities to be followed for Oncology products    0  16
FOR DISSOLUTION CHEMICAL CALIBRATION WE USE PREDNISONE USP.. WHAT IS THE LOT NUMBER OF PREDNISONE? LABEL CLAIM OF PREDNISONE ? HOW MANY SAMPLES IN CONTAINER GENERALLY? reddy-labs   1  33
which std you used for chemical calibration in dissolution? reddy-labs   1  36
Tolerance limit for dissolution media rpm sampling point.    0  12
What is carry over limit in related substance method.    0  28
Why we selecting 900 ml dissolution medium perticular drug as per I.P, USP? torrent-pharma   1  45
How to calculate the RRF value in HPLC analysis. cipla   1  38
using of chemical standards in HPLC he customer gave 100.2% what potency i will use this potency in hplc? vivimed-labs   0  27
What is the difference between Blend uniformtiy and content uniformtiy ?    0  31
How to set impurity limits for Related substances test.    0  41
Why mineral oil or light liquid paraffin is used for ir analysis    0  44
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  77
please explain the job responsibilities of quality assurance..    0  80
how many injection of any concentration should be injected to determine the LOD/LOD?    1  334
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Un-Answered Questions
 
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Give an example of how you've handled a problem patient. 362
concomitant administration of 6-mercaptopurine and which product results in severe bonemarrow suppression? 446
i am preparing for Drug inspector exam.If u have previous questions please send me. 762
What are the filing requirements for ANDA-USA, Europe, Brazil, South Africa, Japan and Emerging Markets 890
What is carry over limit in related substance method. 28
What is the technology transfer and how is it done? 383
How do you think you would get a physician to switch to drug? 488
What is the calibration of HPLC? 82
what is manual integration in HPLC 218
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 243
How can you fix the known and unknown impurity limit for any drug substance? 117
What should be the LOD of dry syrup? 382
hi i have done my b pharma and now i am working as a managing director in my own manufacturing unit is there any scope overthere 4 me 182
What is the difference between Analytical method validation and Analytical method transfer? 84
What skills have you acquired that would apply to the position of Clinical Data Manager? 544
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