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 Categories >> Sciences >> Health Pharma       
 
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  Question  Asked @ Answers Views     select
 
What is carry over limit in related substance method.  0  7
Why we selecting 900 ml dissolution medium perticular drug as per I.P, USP? Torrent-Pharma   0  13
How to calculate the RRF value in HPLC analysis. Cipla  0  13
using of chemical standards in HPLC he customer gave 100.2% what potency i will use this potency in hplc? Vivimed-Labs  0  15
What is the difference between Blend uniformtiy and content uniformtiy ?  0  16
How to set impurity limits for Related substances test.  0  27
Why mineral oil or light liquid paraffin is used for ir analysis  0  26
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
how many injection of any concentration should be injected to determine the LOD/LOD?  1  313
What diffrence between reviewed by and Checked By Alembic  1  282
post translation modification does not occurs in ... ? Hetero   2  298
Can you please mail me the latest syllabus of UTTAR PRADESH DRUG INSPECTOR entrance exam and UTTAR PRADESH FOOD INSPECTOR entrance exam with the eligibility criteria for Uttar Pradesh domicile candidates.  0  86
why assay test and loss on drying test should be performed on same day during raw material analysis?? glenmark  0  155
while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that  0  115
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Un-Answered Questions
 
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Why we selecting 900 ml dissolution medium perticular drug as per I.P, USP? 13 Torrent-Pharma
How polarimeter is calibrated? 64  
define the starting material? 321  
What is difference between method validation and method verification? 72  
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  
how quantitative stability is done 234  
why u want to join as a m.r? 400 GSK
what is manual integration in HPLC 209 LUPIN
what is meant by artwork review and handling procedure with an example? 271  
What are the stability zones and stability conditions? 64  
when we calibrate uv for control of wavelength we scan for 200 to 800 nm but we get the result only for some specific wavelength how we confirm for all other wavelength? 346 Strides
How related substance method is developed for new compound which is not official in the pharmacopeia? 364  
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