2026-03-12 2026-03-12 , online online, 690 € plus tax Dr. Katrin Buss https://forum-institut.com/seminar/26092454-extractables-leachables-current-cmc-requirements-in-light-of-the-upcoming-ich-q3e/referenten/26/26_09/26092454-extractables-leachables-cmc-requirements-draft-ich-q3e_buss-katrin.jpg Extractables & Leachables: Current CMC requirements in light of the upcoming ICH Q3E

E&L and CMC compliance: After having participated in the seminar you will be equipped to navigate the upcoming requirements confidently and proactively prepare your organisation for the implementation of ICH Q3E.

Topics
  • Regulatory expectations and CMC requirements (as currently in place to ICH Q3E)
  • Industry strategies for current global E&L requirements
  • ICH Q3E under development: Scope and key principles from an authority perspective
  • From draft to operations: How industry can prepare for ICH Q3E


Who should attend
This seminar is designed for experienced professionals in Regulatory Affairs and CMC who are responsible for regulatory submissions, dossier preparation, and quality documentation. Professionals that need to navigate today's E&L regulatory landscape while anticipating tomorrow's guideline(s) will particularly benefit from participating.
Aims and objectives
This seminar provides you with a comprehensive overview of the draft regulatory framework of the ICH Q3E, specific CMC requirements, and practical implementation strategies based on both authority and industry perspectives.
The seminar covers the regulatory framework and CMC-specific requirements outlined in the draft guideline, including study design, safety assessments, and Module 3 documentation.
Beyond that, the seminar will also explore how ICH Q3E integrates with the existing E&L guidance documents, such as the USP E&L chapters and BPOG, providing a clear understanding of how these standards work together to support a robust global regulatory strategy.

After having participated in the seminar you will be equipped to navigate the upcoming requirements confidently and proactively prepare your organisation for the implementation of ICH Q3E.
Your benefit

After having participated in the course, you are equipped to

  • master current and future CMC-specific E&L requirements ,
  • avoid deficiencies - authority and industry view, and
  • implement a global regulatory strategy.

Extractables & Leachables: CMC requirements - (Draft) ICH Q3E

Extractables & Leachables: Current CMC requirements in light of the upcoming ICH Q3E

CMC compliance: What to do now and what ICH Q3E will bring

Benefits
  • E&L: Regulatory expectations as currently in place to ICH Q3E
  • Global regualtory strategy: Harmonisation with USP chapters + BPOG
  • First-hand information
  • Officially certified: ISO 9001 + 21001

Webcode 26092454

Book now

JETZT Buchen

Speakers


Everything at a glance

Appointment

17/09/2026

17/09/2026

Period

from 9:00 am until 1:00 pm CET - Online training
You may dial in 30 minutes before the lecture starts

from 9:00 am until 1:00 pm CET - Online training
You may dial in 30 minutes before the lecture starts
Venue

online

online

Downloads
Fee
Your contact

Dr. Birgit Wessels
Conference Manager

+49 6221 500-652
b.wessels@forum-institut.de

Details

E&L and CMC compliance: After having participated in the seminar you will be equipped to navigate the upcoming requirements confidently and proactively prepare your organisation for the implementation of ICH Q3E.

Topics

  • Regulatory expectations and CMC requirements (as currently in place to ICH Q3E)
  • Industry strategies for current global E&L requirements
  • ICH Q3E under development: Scope and key principles from an authority perspective
  • From draft to operations: How industry can prepare for ICH Q3E


Who should attend
This seminar is designed for experienced professionals in Regulatory Affairs and CMC who are responsible for regulatory submissions, dossier preparation, and quality documentation. Professionals that need to navigate today's E&L regulatory landscape while anticipating tomorrow's guideline(s) will particularly benefit from participating.

Aims and objectives

This seminar provides you with a comprehensive overview of the draft regulatory framework of the ICH Q3E, specific CMC requirements, and practical implementation strategies based on both authority and industry perspectives.
The seminar covers the regulatory framework and CMC-specific requirements outlined in the draft guideline, including study design, safety assessments, and Module 3 documentation.
Beyond that, the seminar will also explore how ICH Q3E integrates with the existing E&L guidance documents, such as the USP E&L chapters and BPOG, providing a clear understanding of how these standards work together to support a robust global regulatory strategy.

After having participated in the seminar you will be equipped to navigate the upcoming requirements confidently and proactively prepare your organisation for the implementation of ICH Q3E.

Your benefit

After having participated in the course, you are equipped to

  • master current and future CMC-specific E&L requirements ,
  • avoid deficiencies - authority and industry view, and
  • implement a global regulatory strategy.

Detailed programme

from 9:00 am until 1:00 pm CET - Online training
You may dial in 30 minutes before the lecture starts

Welcome, introduction, expectations


Dr Katrin Buss

Regulatory expectations and CMC requirements (as currently in place to ICH Q3E)
  • E&Ls studies: When and what is required?
  • Analytical methods and validation requirements
  • Safety assessment and toxicological evaluation
  • Documentation requirements for regulatory submissions (CTD Module 3)
  • Assessment perspective: What regulators look for in submissions
  • Common deficiencies and how to avoid them

Biobreak


Samo Kuzmic

Industry strategies for current E&L requirements
  • Global E&L landscape: Navigating requirements and expectations across major regulatory markets
  • Designing robust E&L studies: Practical testing strategies that meet regulatory and technical needs
  • Material selection, qualification, and supplier management (CMC perspective)
  • Structuring E&L data in CTD Module 3: Best practices
  • Cross-functional workflows: Coordinating RA, CMC, analytical, and toxicology teams

Dr Katrin Buss

ICH Q3E under development: Scope and key principles from an authority perspective
  • Scope of application
  • Risk-based approach and quality risk management principles
  • Integration with existing ICH guidelines (Q3A-D, Q6A, M7)
  • Timelines and transition considerations
  • Further perspectives and ongoing developments

Biobreak


Samo Kuzmic

From draft to operations: How industry can prepare for ICH Q3E
  • End-to-end workflow for manufacturing components
  • Packaging and delivery components/systems workflow
  • Safety assessment workflow
  • Lifecycle management
  • Global harmonisation in practice: How ICH Q3E integrates with existing E&L frameworks, including USP <1663>, <1664>, <1665>, <665>, and BPOG
  • Lessons learned and next steps for implementation

Recap and Q&As

End of seminar


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