RegulatoryOfficial
New and updated marketing authorisations for human medicines in July 2026 (Ravimiamet)
🇪🇪 Ravimiamet · Wed 04 Nov 2026
Ravimiamet (the Estonian Medicines Agency) published an overview of newly registered and updated marketing authorisations for human medicines. The title refers to July 2026, but the description refers to late October and early November 2026, so the period covered is unclear. It is a routine administrative listing that is useful for tracking national authorisation status, and the input names no specific products or safety actions.
Official source: Ravimiamet ↗
Summary written by VigiEye from the official notice. AI-assisted; check the source before acting.
More Regulatory
All →
BeyondSpring wins FDA Fast Track for plinabulin-docetaxel in post-immunotherapy NSCLC as cash dwindles to $0.6M
BeyondSpring, Inc. · Fri 13 Nov 2026
Imricor starts US launch of NorthStar iMR system after paediatric FDA clearances
🇺🇸 Imricor Medical Systems, Inc. · Fri 13 Nov 2026
Beyond Air reports record $2.3M quarterly revenue as FDA reviews second-generation LungFit PH
🇺🇸 Beyond Air, Inc. (XAIR) · Fri 13 Nov 2026
FDA sets 10 March 2027 goal date for Intellia's one-time hereditary angioedema gene-editing therapy
🇺🇸 Intellia Therapeutics, Inc. (NTLA) · Fri 13 Nov 2026
BeyondSpring wins FDA Fast Track for plinabulin plus docetaxel in post-immunotherapy NSCLC
🇺🇸 BeyondSpring Inc. (BYSI) · Fri 13 Nov 2026
FDA grants NeOnc Type B meeting on accelerated approval path for intranasal NEO100
🇺🇸 Neonc Technologies Holdings, Inc. (NTHI) · Fri 13 Nov 2026