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

Regulatory Affairs and CMC Conference

Online-Seminar

Ab 1.290,00 € zzgl. MwSt.
Leistungen & Ablauf

Buchungsdetails

Online-Seminar

Ab 1.290,00 € zzgl. MwSt.
Leistungen & Ablauf

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

Sebastian Bergmann

Sebastian Bergmann

STADA Arzneimittel AG,
Bad Vilbel, GERMANY

Head Global RAMACA Systems & Regulatory Operations

Dr. Andreas Bonertz

Dr. Andreas Bonertz

Regulatory Affairs Expert, Langen, GERMANY

Dr Bonertz heads the Clinical Trials Unit of a federal institution, which is responsible for the authorisation of vaccines and biomedical medicinal products.…

Dr. Axel Korth

Dr. Axel Korth

Corporate Counsel - Commercial, Biocon Biologics, London, ENGLAND

Dr. Axel Korth is a senior life sciences lawyer with experience both as an in-house legal counsel as well as in private practice. Axel…

Dr. Ajda Podgoršek Berke

Dr. Ajda Podgoršek Berke

Sandoz Global Development, Ljubljana, SLOVENIA

Regulatory Affairs Specialist as an APIC representative
Ajda Podgorsek Berke, has a PhD in organic chemistry and more than 20 years of overall experiences…

Marcus Savsek

Marcus Savsek

- requested -
Expert for Pharmaceutical Quality & Pharmacokinetics, Bonn, GERMANY

After studying pharmacy, Marcus Savsek worked in the development department of Madaus AG. Since 2001, he has been an…

Angela Schütz, MA

Angela Schütz, MA

Austrian Agency for Health and Food Safety (AGES), Vienna, AUSTRIA

Department Regulatory Affairs, Institute for Marketing Authorisation of Medicinal Products & Lifecycle Management
Angela Schütz, MA is…

Dr. Veronika Schwarz

Dr. Veronika Schwarz

Sandoz GmbH,
Kundl, AUSTRIA

Senior Director from Sandoz as an APIC representative
Veronika Schwarz is a Senior Director leading the API Registration team Austria at Sandoz. She brings over a decade of…

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

Welcome, introduction, expectations

09:15

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
Sebastian Bergmann
  • AI in regulatory affairs: Opportunities, challenges, and lessons learned
  • Structured content management: Use cases and benefits for automation

11:15

Biobreak

11:30

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

12:30

Lunch Break

13:15

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
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
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

Biobreak

16:15

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

17:15

Outstanding questions and final discussion

17:30

End of conference
09:00

Welcome, introduction, expectations

09:15

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

Sebastian Bergmann

  • AI in regulatory affairs: Opportunities, challenges, and lessons learned
  • Structured content management: Use cases and benefits for automation
11:15

Biobreak

11:30

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
12:30

Lunch Break

13:15

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

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

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

Biobreak

16:15

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
17:15

Outstanding questions and final discussion

17:30

End of conference

Downloads

Request the documents using our form.

Prospekt

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

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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

In-house Offers - On-site and Online

We also conduct this seminar exclusively for your company - individually tailored to your requirements, flexible scheduling and available as either on-site or online format. Contact us and we will prepare a customized offer for you.

Request a quote

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Our rating in 2025

Our rating in 2025

More than 3,700 customers have rated our training courses. Thank you for awarding us 4.4 stars out of 5.

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Your Contact Person

We are happy to advise you personally and individually.

Our further education offerings are comprehensive. We are happy to personally match your requirements with our offerings. Let our further education experts advise you and contact us today.
Jean-Marie Bayhurst

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