News dal mondo

20

Feb

US FDA: svolta storica: basterà un solo studio registrativo per approvare i nuovi farmaci

La Food and Drug Administration cambia paradigma: per l’approvazione dei nuovi farmaci sarà sufficiente un unico studio adeguato e ben controllato, superando la storica prassi dei due trial registrativi...[PharmaStar]

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...