From Friday, 12 April 2024 (18:00 CEST) Monday, 15 April 2024 (7:00 CEST), you will experience downtime of IRIS (including IRIS Customer Relationship Management (CRM) software, Industry and Network Portal).
During this period, EMA will load data of Nationally Authorised Products (NAPs) for Human use and Centrally Authorised Products (CAPs) for Human use from its internal database and extended EudraVigilance medicinal product dictionary (XEVMPD) database to Product Management Service (PMS).
This is a crucial step in making further ISO-IDMP compliant, structured and standardised human medicines data available to be used in other EMA systems. This includes the updated CAPs* availability for the web-based Human variations electronic Application Form (eAF) in April 2024 and the upcoming launch of the PMS Product User Interface (view-only, edit functions available later) in May 2024. 
Thank you for your attention and cooperation.
*Including split & match-merge processes. Please refer to EU IG (Implementation Guide) Chapter 7 for a detailed description of these steps.