Details of the US FDA’s warning letter on Lupin has come out. US FDA has asked Lupin to provide the corrective action plan to improve the outer specification, investigation in all facilities, updated lab investigation procedure and also performing retrospective review of the batches which have to be shipped to the US. US FDA has also pointed out the repeated observations that have taken place in Goa as well as Indore on invalidating of outer specification results. Watch the video to know the complete report.
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