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FDA approves Zenbexus for multiple myeloma; NSAI seeks buyer for its MDR notified body business

Published

17 August 2026

Topic

opportunities

Sectors

Biotech

Geography

United States

Source

Read at raps.org

Verified

Fusion42 · 17 August 2026 · Fusion42 review

The US FDA granted accelerated approval to Bristol Myers' drug Zenbexus for multiple myeloma, marking a significant regulatory milestone in cancer treatment. Meanwhile, NSAI is looking for a buyer for its MDR notified body business, indicating a strategic shift in European medical device regulatory support.

This Wire brief sits within Fusion42's coverage of Biotech, and 12 sources have reported it between 13 Aug 2026 and 17 Aug 2026.

◆ The Wire takeaway

Your biotech firm's path to US market access just got clearer with an FDA green light for a new myeloma drug, while shifts in European notified body services open a gap in MDR certification you might fill.

Coverage

12 sources · first reported 13 Aug 2026 · latest 17 Aug 2026

Topics

BiotechFDAmultiple-myelomadrug-approvalmedical-devicenotified-bodyMDR