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Question Asked @ Answers Views     Select
from hplc chromatogram how can we say that calibration is needed now?    0  21
diffrence between known impurity and specified impurity?    0  20
Tolerance limit for dissolution media rpm sampling point.    0  35
using of chemical standards in HPLC he customer gave 100.2% what potency i will use this potency in hplc? vivimed-labs   0  53
How to set impurity limits for Related substances test.    0  61
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  99
please explain the job responsibilities of quality assurance..    0  99
while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that    0  141
How to register or submit drug master file to any regulatory agency?    2  401
what is the disintegration time of mouth dissolving tablet unimarck-pharma   2  481
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  474
what is the mechanism of action of local anaesthetics?    0  179
What is the different between GMP & cGMP ?    1  516
What are the significance of MKT in stability study. alembic   1  951
Which types of deviations are followed in pharmaceuial API manufacturing industry? laurus   0  576
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Un-Answered Questions
 
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What are the regulatory commitments in markets like USA, Canada, Europe, Brazil, South Africa and Japan 296
What are your intentions towards the uplift of the hospital. 321
while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that 141
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. 245
Tolerance limit for dissolution media rpm sampling point. 35
why an employee go for medical representative instead of quality? 271
what is the mechanism of action of local anaesthetics? 179
plz.mail me model papers of drug inspector of chhattisgarh..or MP.if Posible. Mail Id-recha_1428@rediffmail.com...mrs_1428@rediffmail.com, 574
What skills have you acquired that would apply to the position of Clinical Data Manager? 550
What experience do you have in training? 335
what is your experience in medical continuing education. 339
How are you qualified for the position of Assistant Clinical Director? 452
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... 292
what is meant by artwork review and handling procedure with an example? 282
What is the basic requirement for preparing drug master file , like EDMF , USDMF ? 521
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