If we get 100% assay of an Initial sample ,and the stability studies of the same sample got 90% dissolution result, and when the same stability sample was analyzed for RS studies no impurities was found .
Where the 10% Active substance were gone during dissolution analysis.Please help me in getting the conclusion.
how you can fix the known and unknown impurity limit for any
Why should we not dispatch the reprocess material to export?
What aspect of your communications skills have you improved
the most in and how did you accomplish this improvement?
how to select HPLC column for a particular product
why we are using toluene in resolution in UV calibration
How impurity is analyzed in any tablet?
how many clauses are there in iso? give me the clauses
what is your perception of a typical day for a
what is your experience in medical continuing education.
I am studying Bpharmacy final year.
1)I want to interview questions for facing basic
interview.please help me to provide model papers for all
pharma companies and give ur valuable suggestions also.
2)Send me important links for BPharmacy interviews.
3)How should i prepare for facing interview,please give me
My email id:firstname.lastname@example.org
from hplc chromatogram how can we say that calibration is needed now?
what is the defination of Change Control given in various