Real-world evidence
Real-world evidence
Real-world evidence
Memantine product-specific bioequivalence guidance
Orphan designation: Induced pluripotent stem cells-derived myogenic progenitor cells Treatment of Becker muscular dystrophy, 22/05/2025 Positive
Posaconazole product-specific bioequivalence guidance
Infosheet: EMA review of real-world data studies from September 2021 to February 2025
Real-world evidence framework to support EU regulatory decision-making: 3rd report on the experience gained with regulator-led studies from February 2024 to February 2025
eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) training course for sponsors - September 2025, Online, from 29 September 2025, 09:00 (CEST) to 30 September 2025, 13:30 (CEST)
Reflection paper on lessons learned from the COVID-19 pandemic: Scientific considerations on non-clinical aspects
We are pleased to announce the release of the EFIM Annual Report 2024.
The report highlights our key achievements, activities, and collaborations over the past year, reflecting EFIM’s continued commitment to advancing internal medicine across Europe.
Read EFIM Annual Report here!
ICH E20 guideline on adaptive designs for clinical trials - Step 2b