How related substance method is developed for new compound
which is not official in the pharmacopeia?
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What should be the minimum limit of a working standard?
In KF Standardization why we use Disodium Tartarate?
If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can you precede calibration?
What is the difference between uniformity of content and content uniformity as official test for all tablets?
why u want to join as a m.r?
What exepients are used in dry powder injections?
Give details of pilot plant?
What is the wavelenght of sodium D-line in Polarimeter?
What is the difference between mix-up and cross-contamination?
what is stationary phase
Why and when RRF is required to be known in RS Method? How is it helpful during method development?
Why disintegration of uncoated tablets is 15 minutes why not 16 or 14 or any other value .