in api coa contains only process impurities and in product coa contains degradation impurities?
No Answer is Posted For this Question
Be the First to Post Answer
Defination of ZEEMAN EFFECT in NMR ?
how a particular wavelength can be different for a particular compund while analysing by uv and by HPLC.
why require to add enzymes in capsules dissolution only? is it require to tablet also?
Please do not join if u got offer in oncotherapies ltd (STRIDESARCOLAB)especially Mr.Mahesh Bhatt team because job is not secure his team and doesn't have confidence on him becareful this offer?
why we use polystyrene film for ftir calibration?
In the HPLC Calibration done wavelength accuracy done between 200nm-280nm .but not done remaining 300-400nm not done ?
What is the formula for relative diffrence for standard solution in solution stability in validation?
In Dissolution Test why limit is define Q+5% what is the role of +5%.
mahagenco syllabus for the post of chemist
0 Answers MahaGenco, Unimarck Pharma,
Weight balance variation limit during analysis
7 Answers Amneal Pharmaceuticals,
Why sodium lamp is used in polarimeter?
1 Answers Aurobindo, Micro Labs, Mylan,
How can we detect a compound in hplc which does not have any chromofore?