U.S. FDA Approves Streamlined Patient Monitoring Requirements & Removal Of REMS Programs From Bristol Myers’s Cell Therapy Labels
ReutersJun 27, 2025 2:09 AM
June 26 (Reuters) - Bristol-Myers Squibb Co BMY.N:
U.S. FOOD AND DRUG ADMINISTRATION APPROVES STREAMLINED PATIENT MONITORING REQUIREMENTS AND REMOVAL OF REMS PROGRAMS WITHIN BRISTOL MYERS SQUIBB’S CELL THERAPY LABELS
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