Yves Samson
Kereon
Referent:innen
Dr Wolfgang Schumacher
formerly F. Hoffmann-La Roche
Michael Wegmann
F. Hoffmann-La Roche
Dr Bob McDowall
R.D. McDowall Ltd.
Frank Behnisch
Formerly CSL Behring
Dr Arno Terhechte
GMP inspectorate / Bezirksregierung Münster
All times mentioned are CEST.
Hintergrund
In an initial concept paper on the planned revision of the EU GMP guideline Annex 11 ‘Computerised Systems’ in November 2022, the planned changes and content of the new document became clear. Originally planned for the end of 2024 and expected for months, the draft revision of the EU GMP Guidance Annex 11 ‘Computerised Systems’, the draft of the completely new Annex 22 ‘Artificial Intelligence’ and the draft revision of Chapter 4 ‘Documentation’ were presented at the same time on 7 July 2025. All 3 documents can be commented on until 7 October 2025, preferably by ‘Stakeholder Organisations’ but also by anyone else.
The event will mainly focus on the draft of Annex 11 and its links to Chapter 4 ‘Documentation’. Although only a draft, the contents of the final document are clearly recognisable in the document. Therefore, in addition to a critical presentation of the document, missing topics as well as possible consequences for pharmaceutical practice will be discussed.
The event will mainly focus on the draft of Annex 11 and its links to Chapter 4 ‘Documentation’. Although only a draft, the contents of the final document are clearly recognisable in the document. Therefore, in addition to a critical presentation of the document, missing topics as well as possible consequences for pharmaceutical practice will be discussed.
Zielgruppe
The event is aimed at employees from the pharmaceutical and medical devices industry and their suppliers. It is aimed at employees who deal with current regulatory developments on IT in the European Environment.
Date & Technical Requirements
Date of the Live Online Training
Tuesday, 04 September 2025, 09.00 - 18.00 h CEST
Friday, 05 September 2025, 09.00 - 17.00 h CEST
We use WebEx for our live online training courses and webinars. At https://www.gmp-compliance.org/training/online-training-technical-information you will find all the information you need to participate in our trainings and you can check if your system meets the necessary requirements to participate. If the installation of browser extensions is not possible due to your rights in the IT system, please contact your IT department. WebEx is a standard nowadays and the necessary installation is fast and easy.
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.
Programm
Gesamtes Programm als PDF herunterladen
The Live Online Training will deal in detail with all contents of the draft Annex 11. All chapters will be dealt with according to a standardised scheme.
- What are the contents of each chapter?
- Which points are good, which points need to be changed / improved?
- Which points are missing in the chapter?
- Comparison of the requirements in the currently valid Annex 11 with the draft of the new version
- What problems could arise from the new requirements for operational practice?
Chapters in the new draft of Annex 11
1./2. Introduction (Scope / Principles)
Cross-relation to Chapter 4 ‚Documentation ‘
3. Pharmaceutical Quality System
4. Risk Management
5. Personnel and Training
6. System Requirements
7. Supplier and Service Management
8. Alarms
9. Qualification and Validation
10. Handling of Data
11. Identity and Access Management
12. Audit Trails
13. Electronic Signatures
14. Periodic Review
15. Security
16. Backup
17. Archiving
| ECA-Member*: | € 1890,- |
| Non ECA Member*: | € 2090,- |
| EU/GMP Inspectorates*: | € 1045,- |
| APIC Member Discount*: | € 1990,- |
Alle Preise zzgl. MwSt. Wichtige Hinweise zur Umsatzsteuer.
* auch unkompliziert per Kreditkarte bezahlbar
Weitere Termine vor Ort
Weitere Termine vor Ort nicht verfügbar
Aufzeichnung nicht verfügbar
This course is part of the GMP Certification Programme "ECA Certified Computer Validation Manager"
Haben Sie noch Fragen?
Wir stehen Ihnen für weitere Auskünfte gerne zur Verfügung.
E-Mail: info@concept-heidelberg.de
Teilnehmerstimmen
Seminarprogramm als PDFTeilnehmerstimmen - das sagen andere über unsere Seminare:
