Regulatory News March

The European Medicines Agency has announced that the registration for the upcoming “Technical workshop on real-world metadata for regulatory purposes” taking place on the 12th of April is now open. If you wish to register, please send an email to pr@emwa.org and we will share the registration form with you.

• RMP Annex I no longer required
• EMA’s latest publications on COVID-19 vaccines
• EMA public stakeholders meeting on the approval, safety monitoring and impact of COVID-19 vaccines in the EU to be held virtually on 26 March from 13:00 to 15:15 CET