European Commission Launches Public Consultation on Medical Devices and In Vitro Diagnostics Regulations
The European Commission has launched a public consultation on medical device regulations. Participate by March 21, 2025, and contribute to their evaluation.
EMA launches a public consultation on the use of real-world data in the regulation of medicines.
The EMA opens a public consultation on the use of data in the regulation of medicines under the Data Quality Framework for the Regulation of Medicines.