News dal mondo

17

Mar

EMA Management Board: highlights of March 2026 meeting

Board adopts Agency’s 2025 annual report and notes electronic product information implementation roadmap

  • EMA annual report 2025

  • Preparations for implementation of the new EU pharmaceutical legislation

  • Electronic product information implementation roadmap

  • EMA reports on stakeholder engagement activities 2024-2025

  • Monitoring EMA’s independence policies

  • Impact of war in the Middle East

  • Executive Director vacancy notice

  • Clinical trials in the EU

18

Giu

AIFA Sistema informatico Workflow Officine Materie Prime - Ulteriore Aggiornamento tecnico 18 maggio 2026

Formati files ammessi: PDF editabile o p7m. Scansioni a 200 dpi, anche in bianco e nero, per ottimizzare...

15

Mag

US FDA’s New AI-Informed Inspection Pilot and What It Means for Industry

We have written on this blog about FDA’s modernization agenda from several angles lately—from...

15

Mag

EU Regulators discuss new pharma legislation, AI, and more

A panel of European regulators answered questions during a town panel discussion at RAPS Euro Convergence...

15

Mag

US FDA official details top observations from QMSR inspections

The top observations identified in Form 483 reports from inspections conducted under the recently implemented...