Posted on 15 Mar 2021

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 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