Home » BMS Warning Resolved, Path to Nulojix Approval Clear
BMS Warning Resolved, Path to Nulojix Approval Clear
June 10, 2011
In a recent closeout letter, the FDA told Bristol-Myers Squibb (BMS) that the corrective actions BMS has taken at its Manati, Puerto Rico, facility “sufficiently addressed” concerns raised in an August 2010 warning letter, paving the way for approval of BMS’ kidney transplant drug Nulojix.
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