A comprehensive view of european medicines agency (ema). This page highlights a small sample of our full coverage.
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Recent Articles

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Phase 3 study of Roche's OCREVUS subcutaneous injection shows near-complete suppression of multiple sclerosis relapse activity and lesions; approval anticipated from FDA and EMA in 2024
Published: April 17, 2024 by F. Hoffmann-La Roche Ltd. (Roche)
Bristol-Myers Squibb receives EMA's positive opinion on anemia therapy, bolsters collaborative health initiatives, and continues technological advancement in disease treatment
Published: February 24, 2024 by Industry Intelligence Inc.
FDA grants priority review to Regeneron's BLA for linvoseltamab as a treatment for multiple myeloma, decision date is set for August 22, 2024; European medicines agency accepted the drug for review earlier this month
Published: February 21, 2024 by Regeneron Pharmaceuticals Inc.
Bristol Myers announces acceptance of US and EU regulatory filings for neoadjuvant opdivo (nivolumab) and chemotherapy followed by surgery and adjuvant opdivo in resectable non-small cell lung cancer
Published: February 07, 2024 by Bristol-Myers Squibb Co.
Regeneron announces European Medicines Agency has accepted for review the Marketing Authorization Application for linvoseltamab to treat adult patients with relapsed/refractory multiple myeloma
Published: February 02, 2024 by Regeneron Pharmaceuticals Inc.

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