why we are using toluene in resolution in UV calibration
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How to select temperature of ODT in disintegration test
What is main of k*abs in uv visible spectroscopy
Disintegration time for soluble tablet
Why and when RRF is required to be known in RS Method? How is it helpful during method development?
What is your work experience in pharmaceutical field?
What are the steps for the sterilization procedure for Dry Powder injection facility (from Starting)?
Why should we not dispatch the reprocess material to export?
how many types of deviations? describe
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How quantitative stability studies are done?
what are the limit of LOD and LOQ
What is limit of uniformity of content as per USP?