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USP focuses on novel approaches for creating standards that are useful for the manufacture of the growing array of complex biologics. Validation and verification of analytical procedures both play a critical role in a manufacture’s quality control activities in the laboratory. The USP-NF provides guidance on validating non-compendia procedures. USP 857 has been a compulsion from 1st May 2016. They ...
Read More »Is USP chapter 857 an Important Amendment to be Followed in Your Spectrophotometer?
