How impurity is analyzed in any tablet?
How polarimeter is calibrated?
Why and when RRF is required to be known in RS Method? How is it helpful during method development?
What are the stability zones and stability conditions?
What is the difference between Deviation and Out of Specification?
How to conduct Literature Survey for Generics Development for European Market
how many injection of any concentration should be injected to determine the LOD/LOD?
what is purpose of slow,medium,fast sampling in process validation ?
besides Signal & noise ratio how calculating LOD & LOQ?
0 Answers Dr Reddys, Jubilant,
why should we not dispatch the reprocess material to export
how to select HPLC column for a particular product
what is the exact classification of pharmaceutical industry (area wise) as per cleaning limits(Class A.B.C.D)
why we are selecting dissolution media 900ml