at what interval Ukrainian audit will come once you register
your product??
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How we fix the validity period of a volumetric solution and re-standardization due date?
how quantitative stability is done
Why we use basket in place of bowl in dissolution apparatus
what is difference between temporary change control and deviation
What are the limits for LOD and LOQ?
For dissolution chemical calibration we use prednisone usp.. What is the lot number of prednisone? Label claim of prednisone ? How many samples in container generally?
What is the technology transfer and how is it done?
What is the difference between Deviation and Out of Specification?
i like to know when is drug inspector exam 2009.and plz send me da question paper, interviev questions,and other details on my mail.id. shubhg2009@gmail.com. plz
In dissolution test why sample is withdrawn from top of the paddle and not less than 1 cm away from wall?
Why and when RRF is required to be known in RS Method? How is it helpful during method development?
What is the limit for friability of tablets?