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In pharmacopeal solibility parameter of a material, is et
essential to test all paramete? If 70-75% parameter passes
can we assess that the material is satisfactory or not?
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- Aurobindo, I also Faced
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give clarity of linearity and range in method validation
What is the difference between STANDARDIZATION and CALIBRATION of instrument like KF? why do we standardization of KF everyday? Why the KF factor being only 5.02 etc?
5 Answers AlpaMed, Vergo pharma research,
Why we are using K2Cr2O7 for control of absorbance in UV?
When we r doing processing method for sst in Empower software by HPLC, What value has to give in void volume and as per which pharmacopia!
How can v calibrate ftir ? Plz explain me
While performing TOC sst analysis Zero shift disabled & sample analysis zero shift enabled why?
what are the basic requirement for the WHO audit?
why we conclude the area% for the chromatographic purity?
1 Answers Amneal Pharmaceuticals, Lupin,
effect of Ph during analytical run ?
1 Answers Lambda Therapeutic Research,
effect of pore size, pore volume, partical size, column length, carbon load on retention time? what is carbon load? what is the use?
In capadity factor formula is K'= (RT of main compound/RT of first eluted peak)-1 in this formula what is 1
How we can identify process related and degradation impurity in single method with short period?
Organic Chemistry 
