Regulatory Affairs and CMC Conference
Regulatory and quality update and current challenges - 2026
- First-hand information from international authorities/organisations
- Update on ICH M4Q(R2)
- Insights into EU regulatory & CMC developments
Officially certified according to ISO 9001 + 21001

Online-Seminar
Ab
1.290,00 €
zzgl. MwSt.
Leistungen & Ablauf
Veranstaltung - 1.290,-€ zzgl. MwSt.
The participation fee includes documentation for download, a certificate, access to the Learning Space and technical support including PreMeeting.
Period:
from 09:00 am until 05:30 pm CET
Buchungsdetails
Online-Seminar
Ab
1.290,00 €
zzgl. MwSt.
Leistungen & Ablauf
Veranstaltung - 1.290,-€ zzgl. MwSt.
The participation fee includes documentation for download, a certificate, access to the Learning Space and technical support including PreMeeting.
Period:
from 09:00 am until 05:30 pm CET
The event will cover recent updates and practical implications of the EU pharmaceutical legislation, the application of AI in RA, and the new EU Variation regulation. Additionally, it will address the latest developments in quality (draft) guidelines: ICH M13A + M13B, ICH M4Q(R2), an update on the ongoing discussions on nitrosamine contaminations, and the revision of PACMP, Lifecycle Management.
Your speakers
What to Expect
- Update on the new EU Pharmaceutical Legislation
- AI/Automation in Regulatory Affairs
- New EU Variation Guideline
- CMC aspects of New ICH Guideline M13A and Draft Guideline M13B
- Update from APIC on Nitrosamines and ICH M4Q(R2)
- Revision: "Q&As on Post Approval Change Management Protocols (PACMP)"
Who Should Attend
This online conference is ideal for anyone working in the pharmaceutical industry and dealing with regulatory or CMC matters. Professionals in the following departments will benefit particularly:
- Marketing Authorisation/Regulatory Affairs/CMC
- Quality Assurance/Quality Control/Analytics
Objective of the Event
Are you working in Regulatory Affairs, CMC, or Quality Assurance?
Then don't miss this event.
This conference will address practical questions and provide strategic insights into crucial trends affecting these fields.
Engage in in-depth discussions with our experts and network with your colleagues in the industry.
Your Benefit
- RA and CMC experts from international authorities/organisations share their expertise.
- You obtain advanced practical information relevant to your work.
- The conference also addresses issues beyond your immediate area of responsibility.
Programme
from 09:00 am until 05:30 pm CET
You may dial-in 30 minutes before the session starts
09:00
09:15
Dr Axel Korth
- Status of the procedure and timeline
- Overview of key changes
10:15
Sebastian Bergmann
- AI in regulatory affairs: Opportunities, challenges, and lessons learned
- Structured content management: Use cases and benefits for automation
11:15
11:30
Angela Schütz, MA
- Objectives and core principles of the new guideline
- Overview of the key changes and impact on variation classification and submission
12:30
13:15
Marcus Savsek
- Definition of complex/high risk drug products
- Dissolution Conditions, including optimisation and validation
- Assessment of similarity
14:15
Dr Ajda Podgoršek Berke
- Brief update on nitrosamines
- APIM challenges
- APIC template for nitrosamine risk assessment
- APIC Nitrosamine risk management guidance document
15:05
Dr Veronika Schwarz
- Brief overview of the guideline's evolution
- Key differences between ICH M4Q(R1) and ICH M4Q(R2)
- In-depth exploration of M4Q(R2)
- Anticipated challenges and benefits for APIM
16:00
16:15
Dr Andreas Bonertz
- PACMP: What it is and how it works
- New developments and guidance on PACMP
- Benefits and drawbacks of PACMP
- Strategies to consider
- Experiences with PACMP applications
17:15
17:30
Welcome, introduction, expectations
09:15
Update on the new EU Pharmaceutical Legislation
Update on the new EU Pharmaceutical Legislation
Dr Axel Korth
- Status of the procedure and timeline
- Overview of key changes
10:15
AI/Automation in Regulatory Affairs
AI/Automation in Regulatory Affairs
Sebastian Bergmann
- AI in regulatory affairs: Opportunities, challenges, and lessons learned
- Structured content management: Use cases and benefits for automation
Biobreak
11:30
New EU Variation Guideline
New EU Variation Guideline
Angela Schütz, MA
- Objectives and core principles of the new guideline
- Overview of the key changes and impact on variation classification and submission
Lunch Break
13:15
CMC aspects of New ICH guideline M13A and Draft Guideline M13B
CMC aspects of New ICH guideline M13A and Draft Guideline M13B
Marcus Savsek
- Definition of complex/high risk drug products
- Dissolution Conditions, including optimisation and validation
- Assessment of similarity
14:15
Update from APIC on Nitrosamines
Update from APIC on Nitrosamines
Dr Ajda Podgoršek Berke
- Brief update on nitrosamines
- APIM challenges
- APIC template for nitrosamine risk assessment
- APIC Nitrosamine risk management guidance document
15:05
Update from APIC on ICH M4Q(R2) - What to expect
Update from APIC on ICH M4Q(R2) - What to expect
Dr Veronika Schwarz
- Brief overview of the guideline's evolution
- Key differences between ICH M4Q(R1) and ICH M4Q(R2)
- In-depth exploration of M4Q(R2)
- Anticipated challenges and benefits for APIM
Biobreak
16:15
Revision 1: "Q&As on Post Approval Change Management Protocols (PACMP)"
Revision 1: "Q&As on Post Approval Change Management Protocols (PACMP)"
Dr Andreas Bonertz
- PACMP: What it is and how it works
- New developments and guidance on PACMP
- Benefits and drawbacks of PACMP
- Strategies to consider
- Experiences with PACMP applications
Outstanding questions and final discussion
End of conference
Downloads
Request the documents using our form.

Brochure
Weitere Informationen
Access information and dial-in
Log in to the customer portal at members.forum-institut.de/login with your username (e-mail address) and password. Please ensure that you can access the customer portal prior to the event. On the day of the event, you will kick off your online training in the customer portal by clicking 'Participate' in the respective event.
Required technology
Make sure you are using a current version of your browser. We recommend Microsoft Edge.
You need a reliable Internet connection. Please avoid using a VPN connection.
Also, please ensure that your microphone or headset and camera are in good working order.
Pre-meeting and technology check
Familiarise yourself with our Learning Space and gain the confidence you need by attending one of our free pre-meetings. No registration is required. You will find all the pre-meeting dates and the access information in your customer account. Pre-meeting meetings give you the opportunity to explore our Learning Space. 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.
Benefits of a FORUM Institut training course
FORUM Institut’s all-in-one training platform uses the latest teaching methods.
All our online training courses take place in the Learning Space, our holistic learning environment with many features that promote effective and sustainable learning.
- Live and interactive learning on our Learning Space training platform
- A platform with many features: events rooms, chat, course agendas and documents, surveys, workshop rooms and much more
- Easy surveys with Slido
- ‘Deluxe’ chat: group chats, one-to-one chats, one-to-one video chats
- A central repository for documents and media
- Other services and apps such as Padlet and Mentimeter available directly on the platform
- The perfect marriage of teaching methods and technology
- High level of interactivity with plenty of opportunity for questions
- Continuous support throughout the event to ensure the most effective learning
- Free technical pre-meeting to start off your training on the right foot
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Further Information
Your Contact Person
We are happy to advise you personally and individually.

Jean-Marie Bayhurst
Conference Manager
+49 6221 500-685
j.bayhurst@forum-institut.de









