USP methodology, EP methodology, IP methodology, among three if possible to use one methodology for qualify working standard to use USP, EP, IP ? Please explain...
1543can we Consider the Purity threshold and Purity angle in place of peak purity for the specificity test for method verification
1305is it necessary to do HPLC calibration at wavelength 315nm if we are doing analysis at this wavelangth
1648
Protactinium is a rare and highly radioactive element. How is its radioactivity utilized in various scientific and industrial applications?
if you get peak in blank then what require to do?
why salisylic acid not using now days for disdolution calibration?
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?
Explain how many moles of hcl are present in .70 l of a .33 m hcl solution?
What is protein - according to chemistry?
How can be set a responds factor for evaluating a unknown impurity by HPLC
Give the principle of potentiometer titration.
Which are the diffrent grades of api in pharma?
Define an electro chemical cell. Give one example? : Electrochemistry Corrosion
how the compound separate in coulunm,explain
Why is the indicator eriochrome black(ebt) shows wine red color at the beginning and blue color at the end?
If we do accuracy at same concentration at which linearity planned,what is the need to do linearity separately?
hi friends, dis is ramana reddy.i have been workining in bulk drugs as QC chemist.i would like 2 change d company.but our company didn't give d OFFER LETTER,APPOINTMENT LETTER,PAY SLIP.if any body has these documents along with sample RESUME,pls send 2 my mail id i.e ramanareddy.sdpl@ymail.com
As per ICH related substances stability trend limit from initial to shelf life