Webinar: From SAP ERP to SAP S/4HANA - Major changes from GMP perspective

From SAP ERP to SAP S/4HANA - Major changes from GMP perspective

recorded on 17.09.2019


Costs

Non-ECA Members: EUR 249,--
ECA Members: EUR 199,--

(All prices excl. VAT)

If you have any questions, please contact us:
Tel.: +49 (0)6221 / 84 44 0 E-Mail: info@concept-heidelberg.de

Background
SAP S/4HANA is the latest ERP system from SAP SE. Using SAP S/4HANA as digital core enables companies to transform to an “Intelligent Enterprise”. The maintenance period for SAP ERP 6.0, which is the commonly used system in the Life Sciences Industry nowadays, will expire per end of 2025. Up to then, all affected companies will have to move to SAP S/4HANA as their new ERP system. On top of that, most of the customers must change the underlying database (if not already done), because SAP S/4HANA requires the in-memory database SAP HANA. In addition, SAP provides a completely new user interface. The well-known (but not necessarily loved) SAPGUI interface will be replaced with the SAP Fiori launchpad hosting tiles for running apps.
Will all these changes have an impact on the GMP compliance of SAP?

Educational Objectives
The Webinar aims to focus on the following GMP compliance elements in the environment of SAP S/4HANA:
Moving from SAP ERP to SAP S/4HANA: More than a Release Upgrade?
Validation scope depending on different transition scenarios
Changes in the IT architecture and the impact on GMP compliance
SAP S/4HANA Cloud deployment versus GMP compliance
Functional changes in SAP S/4HANA with relevance for GMP compliance

Target Audience
The targeted audience of this Webinar are responsible managers from QC, QA and IT who are engaged in the transformation from SAP ERP to SAP S/4HANA. It especially addresses collaborators who are responsible for IT compliance, members of an SAP competence center but also employees from the business departments, who are acting as Information Manager combining business requirements and IT capabilities.

Basic knowledge regarding computerized system validation (V model, project phases, document types) is required.

Speaker
Stefan Temps has more than 20 years project experience as a Management Consultant for ERP and IT Compliance in the Life Science Industry. During the last two years he focused on the topics of SAP S/4HANA solution architecture and the impact for Life Sciences companies. Stefan Temps studied Industrial Engineering and Management at the Technical University of Hamburg (Germany). He joined DHC Dr. Herterich & Consultants, Germany, as a Senior Consultant in 1996. In 2004 he became Partner of DHC AG, Switzerland.

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