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.
from hplc chromatogram how can we say that calibration is needed now?
when will andhara pradesh government announces drug
inspector posts and when will be the exam conducted? please
how quantitative stability studies are done?
What are the filing requirements for ANDA-USA, Europe,
Brazil, South Africa, Japan and Emerging Markets
explain the selection criteria of a control
What is limit of uniformity of content as per USP?
In HPLC- wavelength calibration calculation why we are
taking peak height and why should not take peak area?
HOW TO SELECT HPLC COLUMN FOR PARTICULAR PRODUCT.
please tell me croscarmellose sodium usp Water-soluble
substances calculation and give me exmpl
pls send me last two years solved papers of health &
malaria inspector to firstname.lastname@example.org
i am doing a dissolution test then what is the rsd criteria
for the six results obtained after calculation?is there any
reference in any guideline for rsd criteria?
What are your intentions towards the uplift of the hospital.
How can I assign a retest date for solvents e.g. toluene,
hai,i had completed my b.pharmacy.i want the coaching
centres for drug inspector exam at hyderabad,pls help me nd
wen wil b the DI exam conducted in 2012 mostly,pls also
forward the model papers.. pls reply me at
Which types of deviations are followed in pharmaceuial API