ALLInterview.com :: Home Page      
 Advertise your Business Here     
Browse  |   Placement Papers  |   Company  |   Code Snippets  |   Certifications  |   Visa Questions
Post Question  |   Post Answer  |   My Panel  |   Search  |   Articles  |   Topics  |   Errors
   Refer this Site  Refer This Site to Your Friends  Site Map  Contact Us      
   
 
 Categories >> Sciences >> Health Pharma
 
  Pharmacy (280)   Lab Technicians (75)   Health Pharma AllOther (88)
 
Suggest New Category 
 


 

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  7
what are the GLP activities to be followed for Oncology products    0  12
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  29
which std you used for chemical calibration in dissolution? reddy-labs   1  33
Tolerance limit for dissolution media rpm sampling point.    0  10
What is carry over limit in related substance method.    0  27
Why we selecting 900 ml dissolution medium perticular drug as per I.P, USP? torrent-pharma   1  41
How to calculate the RRF value in HPLC analysis. cipla   1  35
using of chemical standards in HPLC he customer gave 100.2% what potency i will use this potency in hplc? vivimed-labs   0  24
What is the difference between Blend uniformtiy and content uniformtiy ?    0  28
How to set impurity limits for Related substances test.    0  38
Why mineral oil or light liquid paraffin is used for ir analysis    0  42
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
how many injection of any concentration should be injected to determine the LOD/LOD?    1  332
E-Mail New Answers        Answer Selected Questions       
 [1]    2  ... 3   ... 5   ... 7   ... 9   ... 11   ... 13   ... 15   ... 17   ... 19   ... 21   ... 23   ... 25   ... 27   ... 29    Next
 
 
 
 
 
Un-Answered Questions
 
 Question Views   Select
 
What is mean by partical size distribution. 251
what is difference between temporary change control and deviation 136
What is the basic requirement for preparing drug master file , like EDMF , USDMF ? 511
what is your perception of a typical day for a pharmaseutical representative? 485
can any one give me the question bank for Lab Technician to appear for my HAAD exam . Please send me the Qs. my mail Id is abdullahraj10@yahoo.com Please help. thks. 322
What experience do you have in training? 329
What was your most difficult experience with this population and how did you deal with it? 323
What is the difference between Validation & Qualification? 61
WHAT IS MEANING OF DEAIATION WITH EXAMPLE 255
What is the difference between Deviation and Out of Specification? 143
what is difference between in drug purity and drug potency 72
i am from orissa .can you please send me the question papers of drug inspector exam of orissa ?my email id is dynamicashu@gmail.com.i've completed my b.pharma can i apply for d.i exam ? 403
Do you think it is possible to rehabilitate? 355
why we are using toluene in resolution in UV calibration 138
what is the mechanism of action of local anaesthetics? 164
E-Mail New Answers        Answer Selected Questions