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Innoxel Lifesciences received USFDA Establishment Inspection Report dated November 4 for unannounced April 13-20 pre-approval inspection of general injectable at Vadodara facility; inspection closed with facility deemed ready for commercial operations, second EIR after July 2025.
Bharat Parenterals Commences US Commercial Supply Via Subsidiary Innoxel Lifesciences
Bharat Parenterals Board Approves ₹139 Crore Preferential Share Allotment
Bharat Parenterals Approves ₹300 Crore Biologics CDMO Facility Expansion