CMDh and other EU updates – February 2026

Last updated 17 February 2026

To view updates, click on the ‘+’ sign below.

DateUpdate(s)
17 Feb 2026New section Meeting with Interested Parties – 19 November 2025 added.
12 Feb 2026New section Guidance for applicants for the preparation of the ‘precise scope’ section of the variation application form added.
10 Feb 2026The following new sections were added:
i) Validation checklist for Type II quality variations
ii) Validation checklist for Type II (non) clinical variations
Meeting with Interested Parties – 19 November 2025

The minutes from the meeting are available at this link.

Links to the presentations from the meeting are provided below:

Presentations
CMDh – CTS Overview
CMDh – MAWP
EUCOPE – DCP Slot Booking
CMDh – Slot Booking
EUCOPE – Variations
EFPIA – Variations Worksharing
CMDh – FAQs on Revised Variations Regulation and Classification Guideline from Industry
EUCOPE – ERA Experience & Challenges
MfE – CEP 2.0 


Guidance for applicants for the preparation of the ‘precise scope’ section of the variation application form

This guidance (Rev 1.0 12 February 2026) aims at supporting applicants in completing the ‘Precise scope and Background for a change, and Justification for grouping, worksharing and classification for unforeseen changes (if applicable)’ section of the Application Form for Type I and Type II variations.

It provides guidance on the information to be included in this section and some examples of changes applied for each of the scopes listed in the Guidelines on the details of the various categories of variation, on the operation of the procedures laid down in Chapters II, IIa, III and IV of Commission Regulation (EC) No 1234/2008 concerning the examination of variations to the terms of marketing authorisations for medicinal products for human use, and on the documentation to be submitted pursuant to those procedures (hereinafter called ‘the Variations Guidelines’).

Source: EMA


Updated PLM Portal eAF Release notes now available

An updated version of the PLM Portal eAF Release notes reflecting bug fixes and updates to web eAF made in the version 1.2.1.5 released to production on 02 February 2026 is now available on the eSubmission PLM Portal eAF web page.

Source: eSubmission


Validation checklist for Type II quality variations

Here, you can view the checklist which was last updated on 10 February 2026

Source: EMA


Validation checklist for Type II (non) clinical variations

Here, you can view the checklist which was last updated on 30 January 2026.

Source: EMA