Dr Arno Terhechte
GMP inspectorate / Bezirksregierung Münster
GMP inspectorate / Bezirksregierung Münster
Körber Pharma Consulting
All times mentioned are in CEST
On 7 July 2025, three important draft documents relating to the EU GMP guidelines were published: the revised version of Annex 11 ‘Computerised Systems’, the new version of Chapter 4 “Documentation” and, for the first time, a separate Annex 22 ‘Artificial Intelligence’. The publication of Annex 22 is a milestone – for the first time, a regulatory document is specifically dedicated to the use of artificial intelligence in GxP-regulated Areas. The aim of this event is to analyse and critically evaluate the requirements of the new draft Annex 22 and to place it in the overall context of the applicable GMP regulations. The impact on existing systems and new requirements for the implementation and validation of AI systems will be examined. A particular focus will be placed on the practical consequences for pharmaceutical companies.
This seminar is aimed at specialists and managers from the pharmaceutical industry as well as their service providers and suppliers. It is particularly aimed at those responsible for quality assurance, production, IT, CSV, digitalisation, regulatory Affairs and project management in relation to AI Systems.
The presentations will be made available to you prior to the Live Online Training as PDF files. After the event, you will automatically receive your certificate of participation.
Seminar Programme as PDF
Introduction and Background to Annex 22
Dr Arno Terhechte
Does Annex 22 close the Regulatory Gap? - The two Sides of the Coin - A Detailed Examination
Dr Arno Terhechte & Stefan Münch
Joint Discussion of Annex 22 – Paragraph by Paragraph
In an interactive format, the two speakers will examine the Contents of Annex 22 step by step – alternating between the perspective of the authorities and that of industry. The aim is to promote a common understanding of the requirements while identifying the practical challenges of implementation.
Topics covered include:
Question and Answer Session and Discussion
Moderated by both speakers
At the end, there will be an opportunity to ask the speakers Questions and discuss specific aspects, such as:
ECA-Member*: | € 490,- |
Regular Fee*: | € 590,- |
EU/GMP Inspectorates*: | € 490,- |
APIC Member Discount*: | € 540,- |
(All prices excl. VAT). Important notes on sales tax.
Please contact us:
Tel.: +49 6221 8444-0
E-Mail: info@gmp-compliance.org