News
🇪🇺 EMA Page 20Latest pharmaceutical news, drug approvals, and EMA regulatory updates
Showing 229–240 of 341 articles
Pharmaceutical Intermediates Market to Reach $57 Billion by 2035 as Generic Drug Manufacturing Drives 4.5% Annual Growth
2 min
Dr. Hannah O'ConnorReuters Pharma Day 1: Key Takeaways for European Markets
general · 6 min
Dr. Elena RossiReuters Pharma EU: Day 1 Key Takeaways for Pharma Leaders
general · 8 min
Dr. Elena RossiBelite Bio Submits New Drug Application for Tinlarebant to Treat Stargardt Disease Following Positive Phase 3 Results
2 min
Dr. Amina FaroukAbivax Presents Obefazimod Phase 3 Data at Digestive Disease Week 2026
2 min
Charlotte MeyerPet Service Holding Reports 2025 Annual Results Amid European Veterinary Regulatory Changes
2 min
Prof. Marcus WebbFemasys Launches FemaSeed Complete Fertility Solution for OB/GYNs at ACOG 2026
2 min
Dr. Elena RossiMauna Kea Technologies Secures CE Mark Under New MDR, Expands European Medical Device Approvals
2 min
Sofia AlvarezPembrolizumab Plus Lenvatinib Shows Promise for Rare Clear Cell Gynecological Cancers in Phase 2 Trial
2 min
Dr. Hannah O'ConnorRoche's Gazyva Receives FDA Acceptance for Lupus Treatment Following Positive Phase III Trial Results
2 min
Prof. Marcus WebbIpsen Receives EU Approval for Ojemda (Tovorafenib) to Treat Pediatric Brain Cancer with BRAF Mutations
Pediatric Oncology · 3 min
Sofia AlvarezReuters Pharma EU: Key Takeaways and Industry Insights
general · 8 min
Dr. Elena RossiPopular topics
- Drug Approvals 1,128 articles
- Clinical Trials 634 articles
- Regulatory Updates 687 articles
- Press Releases 443 articles
- Oncology 443 articles
- Mergers & Acquisitions 105 articles
- Rare Diseases 141 articles
Explore intelligence
- Global markets Cross-region command center
- Company directory Sponsor & marketer profiles
- Drug profiles INN & regulatory status
- Clinical trials hub Stage & therapy filters
- Pipeline programs R&D intelligence
- Patent landscape US & EP IP moats
- Event calendar Congress catalysts
- Regulatory reference Submission types & pathways