Questions and answers on post approval change management protocols (PACMP) - Revision 1
Mandatory use of ISO/ICH E2B(R3) Individual Case Safety Reporting inthe EU: Hands-on training course using the EudraVigilance System, Online, from 23 February 2026 to 26 February 2026
Mandatory use of ISO/ICH E2B(R3) Individual Case Safety Reporting inthe EU: Hands-on training course using the EudraVigilance System, Online, from 16 March 2026 to 20 March 2026
Mandatory use of ISO/ICH E2B(R3) Individual Case Safety Reporting inthe EU: Hands-on training course using the EudraVigilance System, Online, from 13 April 2026 to 17 April 2026
Mandatory use of ISO/ICH E2B(R3) Individual Case Safety Reporting inthe EU: Hands-on training course using the EudraVigilance System, Online, from 18 May 2026 to 22 May 2026
Mandatory use of ISO/ICH E2B(R3) Individual Case Safety Reporting inthe EU: Hands-on training course using the EudraVigilance System, Online, from 15 June 2026 to 19 June 2026
Mandatory use of ISO/ICH E2B(R3) Individual Case Safety Reporting inthe EU: Hands-on training course using the EudraVigilance System, Online, from 26 January 2026 to 30 January 2026
Guidance on good manufacturing practice and good distribution practice: Questions and answers
How to submit information on authorised and investigational medicines
Draft user manual for the eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) user interface (XEVMPDweb)