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
   Testimonials Refer this Site  Refer This Site to Your Friends  Site Map  Contact Us      
   
 
 Categories >> Sciences >> Health Pharma >> Health Pharma AllOther
 
Suggest New Category 
 


 

Question Asked @ Answers Views     Select
from hplc chromatogram how can we say that calibration is needed now?    0  10
diffrence between known impurity and specified impurity?    0  13
Tolerance limit for dissolution media rpm sampling point.    0  29
using of chemical standards in HPLC he customer gave 100.2% what potency i will use this potency in hplc? vivimed-labs   0  41
How to set impurity limits for Related substances test.    0  54
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  92
please explain the job responsibilities of quality assurance..    0  93
while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that    0  133
How to register or submit drug master file to any regulatory agency?    2  371
what is the disintegration time of mouth dissolving tablet unimarck-pharma   2  455
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  457
what is the mechanism of action of local anaesthetics?    0  175
What is the different between GMP & cGMP ?    1  489
What are the significance of MKT in stability study. alembic   1  932
Which types of deviations are followed in pharmaceuial API manufacturing industry? laurus   0  571
E-Mail New Answers        Answer Selected Questions        Post New health-pharma-allother Questions
 [1]   2   3   4   5   6    Next
 
 
 
 
 
Un-Answered Questions
 
 Question Views   Select
 
Do you think it is possible to rehabilitate? 360
Hi Sir?Mam, If i complete SAS CLINICAL in India, can i step forward to USA for job trials? How far is it possible? Am a B.pharm student ,willing to make up my Master's degree too,will this both M.Pharm and SAS help me out to get a job in USA? Please help me out with a good answer. 243
WHAT IS MEANING OF DEAIATION WITH EXAMPLE 269
from hplc chromatogram how can we say that calibration is needed now? 10
Tolerance limit for dissolution media rpm sampling point. 29
why an employee go for medical representative instead of quality? 268
How are you qualified for the position of Assistant Clinical Director? 449
What aspect of your communications skills have you improved the most in and how did you accomplish this improvement? 346
How can I assign a retest date for solvents e.g. toluene, methanol, etc? 402
what is the test scenario? 290
what is meant by artwork review and handling procedure with an example? 280
concomitant administration of 6-mercaptopurine and which product results in severe bonemarrow suppression? 480
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? 285
plz.mail me model papers of drug inspector of chhattisgarh..or MP.if Posible. Mail Id-recha_1428@rediffmail.com...mrs_1428@rediffmail.com, 571
how many clauses are there in iso? give me the clauses details? 560
E-Mail New Answers        Answer Selected Questions