Ralf Gengenbach
gempex
gempex
Roche Diagnostics
GMP Inspector
A GMP inspector establishes the necessary regulatory framework so that artificial intelligence can be used in a GMP-compliant manner. He will provide an insight into the planned changes to Annex 11 and discuss the new Annex 22 on artificial intelligence. An industry representative will then give an overview of the possible applications of artificial intelligence in the area of qualification and validation. Current practical experience in the pharmaceutical industry will be discussed. Another industry representative will then present the use of artificial intelligence in equipment qualification in a "live performance". He will also highlight potential savings. Two question-and-answer sessions will provide the opportunity to discuss this complex topic.
Hardly any other topic is currently being discussed in the pharmaceutical industry as much as the use of artificial intelligence. The potential applications appear to be vast, the uncertainty even greater. There are a lot of terms "buzzing around": artificial intelligence vs. machine learning vs. deep learning. There are Questions:
The one-day online compact seminar "The use of artificial intelligence in qualification and validation" aims to help clarify these Questions.
It is aimed at those interested in the use of artificial intelligence in the field of qualification and validation, but who also want to know which requirements are necessary from an official point of view before use. Explicitly addressed are e.g. quality management/quality assurance managers, validation officers, production managers, etc.
Date of the Live Online Training
Wednesday 24 September 2025, 09.00 - 15.45 h
All times mentioned are CEST.
Technical Requirements
We use Webex for our live online training courses and webinars. At www.gmp-compliance.org/training/online-training-technical-information you will find all the information you need to participate in our events 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.
Gesamtes Programm als PDF herunterladen
The Use of Artificial Intelligence in the Pharmaceutical Environment: a GMP Inspector’s Perspective
Basic Terms
Basic EU Framework Conditions
Specific Requirements
Focus: Testing
The Use of Artificial Intelligence in Qualification and Validation: Possibilities and Limitations - an Industry Representative’s Perspective
Why use Artificial Intelligence for Qualification and Validation?
Free Systems vs. in-house Systems
Previous Experience with the Use of Artificial Intelligence in the Area of Qualification and Validation
Case study: Use of Artificial Intelligence in Equipment Qualification
Creation of a User Requirement
ECA-Member*: | € 1090,- |
Regular Fee*: | € 1290,- |
EU/GMP Inspectorates*: | € 645,- |
APIC Member Discount*: | € 1190,- |
Alle Preise zzgl. MwSt. Wichtige Hinweise zur Umsatzsteuer.
Wir stehen Ihnen für weitere Auskünfte gerne zur Verfügung.
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