Sebastian Bergmann
STADA Arzneimittel AG, Bad Vilbel, GERMANY
Head Global RAMACA Systems & Regulatory Operations
More information please click here.
Gürtay Altinok
STADA Arzneimittel AG, Bad Vilbel
Head of IT Regulatory; As Head of the IT Regulatory Department at STADA, Mr. A is responsible for the RIM platform as well as other key regulatory systems, including the formulation database and the publishing/validation system. With more than 20 years of project management experience, 12 of which in the demanding pharmaceutical sector, he ensures the implementation, maintenance, and smooth operation of these systems in close collaboration with the respective departments.
Christine Hirt
MAIN5 GmbH & Co. KGaA, Frankfurt, GERMANY
Management Consultant & Regulatory Consulting Lead; Christine Hirt is Management Consultant & Regulatory Consulting Lead and responsible for regulatory business consulting at MAIN5. She has more than 20 years of experience in the field of Regulatory Affairs working for industry and authority representatives. Christine is internationally recognized on expert level for regulatory business processes, guidelines and regulations. She is an active member in several associations, such as DIN/ISO TC/WG6, IRISS, BPI and MEGRA. Participating actively in the IDMP adoption expert group of WG6/TC215/ISO and other expert groups associated with implementing RIMS and IDMP.
24 - 25/11/2026
24 - 25/11/2026
each from 9:00 a.m. - 12:30 a.m. CET
online
online
Event - 1,290€ plus tax
The participation fee includes downloadable documentation, a certificate, access to the Learning Space and technical support including PreMeeting.
Event - 1,290€ plus tax
The participation fee includes downloadable documentation, a certificate, access to the Learning Space and technical support including PreMeeting.
Jean-Marie Bayhurst
Conference Manager
+49 6221 500-685
j.bayhurst@forum-institut.de
This seminar covers the key drivers of digital transformation in Regulatory Operations - from data quality and AI-driven automation to IDMP, eCTD 4.0, and ePI. Across two half-day sessions, you will gain practical strategies and discuss real-world use cases with experienced practitioners.
This intensive seminar spanning two half-day sessions provides a comprehensive overview of the digital transformation in Regulatory Operations. From data quality and AI-driven automation to IDMP implementation and eCTD 4.0, all key aspects of a modern, data-driven regulatory landscape will be addressed.
You will learn how to ensure data quality as the foundation for RIM performance and AI-readiness, and how to leverage automation and cloud-based platforms to streamline your regulatory workflows. You will also gain in-depth knowledge of IDMP/SPOR requirements, the transition from XEVMPD, and the upcoming eCTD 4.0 and ePI frameworks.
Through real-world use cases and interactive group discussions, you will be equipped with practical strategies to position Regulatory Operations as a strategic data hub within your organisation.
24.11.2026 09:00 Day 1
24.11.2026 09:00 Welcome & Technical Warm-Up
24.11.2026 09:15
24.11.2026 10:00
24.11.2026 11:00 Coffee Break
24.11.2026 11:15
24.11.2026 12:30 End of Day 1
25.11.2026 08:00 - 09:11 Day 2
25.11.2026 09:00
25.11.2026 10:00
25.11.2026 11:00 Coffee Break
25.11.2026 11:15
25.11.2026 12:30 End of Day 2
You can attend one of our pre-meetings and explore our Learning Space free of charge. Registration is not required. You can find available dates for a pre-meeting in your customer portal. Click the green ‘Participate’ button in the pre-meeting in the customer portal and you will be redirected to the Learning Space.
The pre-meeting gives you the opportunity to explore our Learning Space and to familiarise yourself with the technology to start off your online training on the right foot. This is a non-binding offer for all our customers and not a prerequisite for participation. If a pre-meeting date does not suit you but you would still like a technology check, please contact us.
of 5 stars of all ratings from 2025
of 5 stars on Trustpilot = good
Regulatory expectations regarding risk management for pharmaceuticals in (emerging) markets often contend with the strin...
This online two-day course equips new, aspiring, and practising QPPVs with a clear understanding of their role under EU ...
This seminar explores how artificial intelligence can be effectively and responsibly integrated into regulatory writing ...
Quality & GMP Essentials for Regulatory Affairs/CMC: Managing the interface - knowledge of quality-relevant facts, GMP f...
Would you like to feel more confident presenting your CMC/quality data clearly and in full compliance with regulatory st...
Many abbreviations are used in pharma & healthcare. Download the list of the most important ones.
Details
Try out our e-Learning programmes free of charge and without any obligation.
Details
We are now officially certified to ISO 9001 and ISO 21001 standard.
Details