Interested to Buy Any Domain ? << Click Here >> for more details...
Difference between standard operating procedure and standard test procedures in pharmaceutical industry
2 10004Dear sir, This is R.Kadambavadani working in a pharma industry. while doing RS analysis of ibuprofen API, unknown peak eluting some times in the 0.6 Min RT. Kindly send me what is the exact reason behind that. also am using ACN the mobile phase.
1 2581Post New Analytical Chemistry Questions
what is the disso medium for tropsiun chloride
before starting analytical method valodation what you checking? and how giving preference to start validation?
Why we check moisture,ash & AIA in product
in monograph 7 imp are there but in vendor showing 5 imp do not req to include 2 imp for that what will be justification?
How you develop a method in HPLC?
on the basis of bcs class how to proceed the solubility?
acceptance criteria for lod & loq by standard deviation of response and slope??
why lactose has less charges when packed in steel containers when compared with packing of lactose in polyamide material?
Did anybody have method for acetyl cysteine effervescnce tablet
what is the different in Total ash, sulphated ash, acid insoluble ash, alcoholic or non alcoholic ash?
What is the requirement for brazil in the analytical method vslidation comparr to ich?
Difference between hlaf and rlaf
CAN WE DETERMINE THE PEAK PURITY IN GAS CHROMATOGRAPHY ANALYSIS?
when we talk about change in entropy we consider total entropy means of surround +entropy of system but when we talk about change in Gibss free energy we consider entropy of system.explain with reason.
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
