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 new
   Refer this Site  Refer This Site to Your Friends  Site Map  Bookmark this Site  Set it as your HomePage  Contact Us     Login  |  Sign Up                      
Google
   
 
 Categories >> Sciences >> Health Pharma >> Health Pharma AllOther       
Suggest New Category 
 


 

  Question  Asked @ Answers Views     select
 
using of chemical standards in HPLC he customer gave 100.2% what potency i will use this potency in hplc? Vivimed-Labs  0  15
How to set impurity limits for Related substances test.  0  27
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  64
please explain the job responsibilities of quality assurance..  0  69
while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that  0  115
How to register or submit drug master file to any regulatory agency?  2  317
what is the disintegration time of mouth dissolving tablet Unimarck-Pharma  2  403
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  419
what is the mechanism of action of local anaesthetics?  0  155
What is the different between GMP & cGMP ?  1  441
What are the significance of MKT in stability study. Alembic  1  885
Which types of deviations are followed in pharmaceuial API manufacturing industry? Laurus  0  546
What is the differance Between Calibration & Validation MSN-Pharma  6  1418
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  271
WHAT IS MEANING OF DEAIATION WITH EXAMPLE  0  246
E-Mail New Answers        Answer Selected Questions        Post New Health Pharma AllOther Question
 [1]   2   3   4   5   6    Next
 
 
 
 
 
Un-Answered Questions
 
 Question Views Asked at   Select
 
please e-mail me the model of Tamil Nadu drug inspector question papers 612  
Give an example of how you've handled a problem patient. 356  
What are the filing requirements for ANDA-USA, Europe, Brazil, South Africa, Japan and Emerging Markets 872  
why an employee go for medical representative instead of quality? 260  
what is ur strengths and weekness in ur professional life as medical rep? 686 Ranbaxy
while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that 115  
What are your intentions towards the uplift of the hospital. 305  
how many clauses are there in iso? give me the clauses details? 546  
How are you qualified for the position of Assistant Clinical Director? 438  
what is your experience in medical continuing education. 325  
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? 271  
Which types of deviations are followed in pharmaceuial API manufacturing industry? 546 Laurus
E-Mail New Answers        Answer Selected Questions
 
 
 
 
 
 


   
Copyright Policy  |  Terms of Service  |  Articles  |  Site Map  |  RSS Site Map  |  Contact Us
   
Copyright 2013  ALLInterview.com.  All Rights Reserved.

ALLInterview.com   ::  KalAajKal.com