header-image

(AI) Artificial Intelligence in an GxP Environment - Online Training Recording (2024)

Seminar-Nr. 22014

Referent:innen

Yves Samson

Yves Samson

Kereon

Stefan Münch

Stefan Münch

Körber Pharma Consulting

Stefan Hessel

Stefan Hessel

Reusch Rechtsanwaltsgesellschaft

Daniel Wolf

Daniel Wolf

Universitätsklinikum Ulm

Martin Heitmann

Martin Heitmann

d-fine

Ib Alstrup

Ib Alstrup

Danish Medicines Agency (DKMA)

Dr Juergen Schmitz

Dr Juergen Schmitz

GSK Vaccines

Hendrik Rolshausen

Hendrik Rolshausen

DHC Dr. Herterich & Consultants

Urs Alexander Peter

Urs Alexander Peter

HC Dr. Herterich & Consultants

Felix Georg Müller

Felix Georg Müller

plus10

Zielsetzung

Why should you participate in this event?
  • You will learn the basics of AI / ML and its applicability in the GxP Environment
  • How can pharmaceutical basics, e.g. risk management and qualification / validation be applied to AI? You will experience first approaches!
  • Are relevant pharmaceutical regulations adapted to this new technology and what expectations does an inspector have during an inspection? First concepts will be presented!
  • In case studies, pharmaceutical companies show first practical and practised approaches to the use of AI

Hintergrund

At the latest, Artificial Intelligence (AI) has arrived in the general public since ChatGPT and Bard. Opinions range between absolute euphoria and the invocation of the downfall of humanity. The foundations of AI were laid many years ago and can now be widely implemented due to massively available computing power. The topic has also found its way into the pharmaceutical landscape. First applications have come into operation. The interesting questions here are whether and how this technology is compatible with pharmaceutical regulations, specifications and authorities’ expectations.

Zielgruppe

The Online Training is aimed at managers and QA members as well as engineers from the pharmaceutical industry, suppliers and service companies who qualify and operate AI applications in a GxP environment.

Technical Details

To participate in an on demand training course or webinar, you do not need any software. The recordings are made available via a streaming server. In general, the recording is provided in MP4 format, which any PC (Microsoft Windows, Apple IOS) or tablet can easily display.

Timing and Duration:
When you register for the on demand Training course or webinar you can decide at what date you want to follow the training course online. For a 1-day training course you will have 2 days in which the stream is available (for 2-day training course 3 days and for a 3-day training course 4 days). Within in this timeframe you can start & stop the stream according to your needs.
In time before the scheduled date (your desired date) you will receive an e-mail from us with a link for direct participation as well as your log-in data.

Training Course Documentation and Certificate:
The presentations will be made available as PDF files via download shortly before the online training course. After the event, you will automatically receive your certificate of participation.

Programm

Introduction to Artificial Intelligence (AI)
  • History of AI
  • Types of AI
  • Real life examples
Introduction to Machine Learning (ML)
  • Technological basics
  • Different learning / training methods
  • Example use cases
AI in Image Processing
  • Introduction to deep learning models for imaging
  • Deep learning for diagnosis and prognosis
  • Pre-training of deep learning models
  • Explainable Artificial Intelligence
AI/ML in Pharma, Biotech, and Med Devices
  • Challenges for the Life science industry
  • The GAMP-perspective on AI/ML
  • Use cases / Known scenarios
Regulatory Requirements / Concerns / Assessment
  • Pharmaceutical laws
  • EU-GMP Guide Annex 11
  • Inspection strategy
  • What do inspectors expect from the regulated user?
Inspection Readiness
  • Overview of regulatory guidance and evolving inspection practices
  • Overview of supporting processes: data management, risk management, change management
  • Have documentation ready – provide reasoning and justifications
  • How to setup mock inspections successfully
Data and Models
  • Overview of model and data types
  • Data split: training, validation, testing
  • Data quality, representativeness and typical data challenges
  • Use of synthetic data
Introduction to and Application of Generative AI in Regulated Pharma
  • Introduction to Large Language Models (LLM) and example use cases
  • Specialization and tailoring of LLMs in computerized Systems
  • Typical risks when using LLMs
  • Performance evaluation and validation strategies for LLMs
Generative AI - Legal Requirements and practical Implementation
  • AI and law: introduction and overview
  • Outlook and update on the EU AI Act
  • Copyright and trade Secrets
  • Data protection requirements and processing of personal data
  • Practical implementation and best practicess
Validation Approaches
  • Maturity: Increasing autonomy and transferring Control
  • Governance: Developing and operating AI solutions in GxP-regulated areas
The Use of Artificial Intelligence in Pharmaceutical Manufacturing, Developments, Implementation, and Examples
  • Risks and Opportunities
  • Preparing the Quality Management System for AI
  • Where to implement and what to avoid
  • Pactical examples and attention Points
  • Validation requirements
  • Future Developments
Risk Management for AI/ML
  • Basics of a ML Risk and Control Framework
  • Applying QRM to development and operation of AI applications
  • Using hazard clusters to guide the risk process
Efficiency Increase in Pharma Production Lines through GMP-compliant AI Tools – Case Study Review
  • Lessons learned from primary and secondary packaging lines and Auto-Injectors production
  • When continuously learning and situationally acting tools can help and when not
  • Introduction of Use cases for live learning optimization tools in GMP-environment
  • Short Intro: AI-based behavior learning on high frequency machine data of whole production lines
  • Obstacles during validation
  • Learnings from 24/7-operations Integration
  • Review of realistic and unrealistic benefits
Trustworthy AI: Innovative Approaches for Transparency in Validation
  • Black box or partner: How can transparency of AI be increased?
  • Interpretability of AI-based decisions
  • Foundations of Explainable AI
  • Approaches for the validation of AI systems in GxP environment
 
Recording from 29/30 October 2024
Duration of Recording: approx. 10h 14min

ECA-Member*: € 1690,-
Regular Fee*: € 1890,-
EU/GMP Inspectorates*: € 945,-
APIC Member Discount*: € 1790,-

Alle Preise zzgl. MwSt. Wichtige Hinweise zur Umsatzsteuer.

* auch unkompliziert per Kreditkarte bezahlbar
American Express Visa Mastercard

icon
Weitere Termine vor Ort
Weitere Termine vor Ort nicht verfügbar
icon
Weitere Termine online
Weitere Termine online nicht verfügbar

Haben Sie noch Fragen?

Wir stehen Ihnen für weitere Auskünfte gerne zur Verfügung.

Frau mit Headset
Tel.: +49 6221 84 44 0
E-Mail: info@concept-heidelberg.de

Zurück

Teilnehmerstimmen - das sagen andere über unsere Seminare:

"Die Umsetzung mit Memberspot ist wirklich ausgezeichnet gelungen.
Es unterstützt die Wissensvermittlung und gewährleistet auch die richtige Durchführung des Kurses.”
Christian Wagener, WAGENER & CO. GmbH
GMP Basis-Einstiegsschulung (B 1) - Aufzeichnung Online Seminar, April 2024

„Kurzweilig, informativ“
Behrendt, Christian, IOI Oleo GmbH


„Austausch zwischen Teilnehmern & Vortragenden sorgt für Anstöße & Optimierungsmöglichkeiten im eigenen Unternehmen! Praxisnahe Beispiele veranschaulichen und vertiefen die Theorie sehr gut“
Marina Maier, CHEPLAPHARM Arzneimittel GmbH

Abweichungen und CAPA (QS 12)
November 2024

„Danke für das tolle und interessante Seminar! Ich nehme mir fachlich total viel mit und habe viele tolle Menschen kennengelernt.“
Melanie Schifferer, DAIICHI SANKYO EUROPE GmbH
Batch Record Review (QS 23)
September 2024

Guter, breit gefächerter Überblick mit interessanten Verknüpfungen zur Praxis,
welche die Theorie super veranschaulicht.”
Marina Kicoranovic, Labor Hartmann GmbH
GMP/Basis-Einstiegsschulung (B 14), September 2023

Die Referenten waren sehr gut! Sie haben sehr klar gesprochen, nur sehr wenige englische Begriffe
verwendet (super) und waren sehr praxisbezogen.”
Astrid Gießler, Regierungspräsidium Karlsruhe
Live Online Seminar - Basiskurs Computervalidierung & Datenintegrität im GxP Umfeld (B 3), Juni 2023

Sehr guter Bezug zur Schulung für einen GMP-Anfänger. Habe mich sehr gut abgeholt gefühlt.”
Dr. Harald Werner, Infraserv GmbH & Co. Höchst KG
GMP-Basisschulung (B 1), Juni 2023

„Interessante Themen, gut vorgetragen, die eigenen Erfahrungen der Vortragenden helfen, dies noch besser nachzuvollziehen.“ „Gute Gestaltung der Workshops, das Zusammenarbeiten in Gruppen und der Austausch mit anderen hilft sehr.“
Manuela Seibert, Merck, GMP-Leadauditor/in (FA 2), April 2024

NEWSLETTER

Bleiben Sie informiert mit dem GMP Newsletter von Concept Heidelberg!

GMP Newsletter

Concept Heidelberg bietet verschieden GMP Newsletter die Sie auf Ihren Bedarf hin zusammenstellen können.

Hier können Sie sich kostenfrei registrieren.

Kontakt

Kontaktieren Sie uns

Haben Sie Fragen?

Concept Heidelberg GmbH
Rischerstraße 8
69123 Heidelberg

Tel. :+49622184440
Fax : +49 6221 84 44 84
E-Mail: info@concept-heidelberg.de

zum Kontaktformular