How we can identify process related and degradation impurity in single method with short period?
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what is the significant of pH in HPlc?
Why dissolution test is not performed in all of the products
Which are the diffrent grades of api in pharma?
inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?
In GC Why does retention time decrease when temperature increases? Also how does a change in temperature effect selectivity?
What is the function of end capped column?
How would you decide dissolution medium for NCE compound of class I drug
difference between record & document ?
void volume is depending on column or not? if yes how will you depend?
Suppose we prepared pH buffer solution in lab.and calibrate against NIST solution, and same shall going to used upto 30 days. is it possible to stable pH and apperance ? suggest ?
what is the principal of malvern particle sizer & its used in pharma industry
signifcance of detector lenearity in calibration f hplc