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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?
1 5338Why triethylamine and o-phosphoric acid used while setting pH of mobile phase during HPLC Analysis?
6 33627why RID detector is used for selective materials like Mannitol, Hydroxyethyl Starch and Sorbitol?
5 12484For Dissolution test why we are Performing 6 Bowls why not more.any were mentioned or in what basis we are performing? --------Veerabhadrarao.M
2 12153In Number of Theoretical Plates (N) = 16 (tr/w)2. where tr: retention time, and W: peak width. My Question is here in formula what is 16.Can u explain briefly? ---Veerabhadrarao.M
3 19465A new drug substance found fail to meet specification for an unknown Impurity during stability study(Specific change),how would further proceed?
2 7354Post New Analytical Chemistry Questions
WHICH STANDARD WE USE IN SILICA ANALYSIS IN SILICA-GEL METHOD FOR SOLID SAMPLE
what is mean by covalidation
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
How to set analyticl specification for combination products?
how you fix the limits of impurities?
in which situation require to change rs specification?
how you start RS method development when for new product?
Tell me about analytical method validation in QC
What is the calibration of uv process and preparation
acceptance criteria for lod & loq by standard deviation of response and slope??
UV and PDA detector, which have less signal to noise ratio?
Why Ethanol is Used for Standardization of GC Head space?
process of Diclofenac sodium,IP.
Hi sir if any product monograph not given known impurities (may be 5 impurities) specifications then how we require to proceed for inhouse formulation?
what is the disso medium for tropsiun chloride
