3RD ANNUAL GENOTOXIC IMPURITIES SUMMIT: BEYOND NITROSAMINES

Two days of expert insights and high-impact networking with leading toxicologists, regulatory specialists, and pharmaceutical innovators.This is your opportunity to advance your career, stay ahead of evolving regulations like ICH M7, and deepen your expertise in genotoxic risk assessment and impurity control.

berlin

October 1-2, 2025

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Get your seat with €250 off

Featuring industry leaders in genotoxic impurity control and pharmaceutical safety.

About the conference

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event date

October 1-2

Genotoxic Impurities Summit 2025:
The Transformation of Pharmaceutical Safety Through Science and Regulation

The 3rd Annual Genotoxic Impurities Summit is a premier event uniting experts from pharmaceutical companies, regulatory agencies, and toxicology research.
Focusing on critical topics such as nitrosamines control, ICH M7 updates, DNA-reactive impurities, and advanced genotoxic risk assessment strategies, this summit is the ideal platform for professionals aiming to stay ahead in impurity management and enhance pharmaceutical safety standards.

Berlin

Event location

OUR SPONSORS

If you are interested in becoming a partner or sponsor, please feel free to contact us.

Why It’s Worth It?

Meet leading tech and analytics providers through dynamic 5-minute pitches and hands-on demos.
Explore state-of-the-art solutions for impurity monitoring, analytical modeling, and automated compliance tools—directly from the teams behind them.

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Discovering the Latest Technologies

Networking Opportunities

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Start your experience at our exclusive pre-conference networking reception. Connect with toxicologists, chemists, compliance professionals, and regulatory experts in an informal setting.
Receive a curated attendee directory to support strategic follow-up and long-term collaboration after the event.

Explore how pharmaceutical and regulatory pioneers are tackling genotoxic impurities beyond nitrosamines.
Gain firsthand insights from experts at Sanofi, Sandoz, Baxter, and others on the latest in risk assessment, regulatory compliance, and impurity control strategies.

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Sessions from Industry Leaders:

Interactive Workshops & Technical Deep Dives

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Participate in focused technical sessions and case study-led discussions.
Engage with advanced methods for detection, qualification, and mitigation of DNA-reactive impurities across drug substances and excipients.

get the full conference program and a discount on early booking

All materials

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Request the full program and a personalized consultation to learn more about the benefits of participation

What’s in it for you as an attendee?

Networking opportunities

with key stakeholders from pharma, biotech, and regulatory bodies

for managing genotoxic impurities across the drug development lifecycle

Hands-on strategies

into nitrosamines, ICH M7, and the latest regulatory expectations

Cutting-edge insights

We provide the knowledge, networking, and innovation to drive your professional evolution in the pharma sector

«Business Conference Facilitation» is more than just an event organizer

Request your discount

€250
off

brief schedule

Schedule

Evening Reception

17:00-19:00

16:10-16:20

Closing Remarks

15:50-16:10

Prosecco Round Table

12:00-13:00

Lunch

11:50-12:00

Closing Remarks

Opening Remarks

8:30-9:00

9:00-11:50

Sessions

2 days

from 8:00 AM

OCTOBER 1-2, 2025

October 2

October 1

Opening Remarks

9:00-9:10

8:30-9:00

Registration

Sessions

9:10-11:50

Lunch

12:00-13:00

berlin

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Attend the conference from anywhere in the world and gain insights from global experts, access live sessions, join interactive Q&As, and receive post-event materials—all without leaving your desk.

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Contact Us to Enhance Your Conference Experience with Expert Guidance.

Meet Our Speakers

Preclinical Evaluation

Medical Devices

Toxicological Risk

Crystal D’Silva

Associate Director, Preclinical Toxicology | Preclinical Sciences, Strategy, Innovation |

PRINCIPAL RESEARCH SCIENTIST

DR. MICHAEL BURNS

Mutagenic Risk

Small Molecule APIs

Purging Calculations

Department Head

Rok Grahek

Impurity Profiling

Drug Substance Characterization

LC-MS / GC-MS Analytics

Analytical Development

Pharmaceutical QA/QC

ICH M7 Compliance

Thierry Beltran

ICH-M7 Compliance Coordinator within PDP Scientific Excellence

Senior Market Development Manager Pharma/CRO

Nando Sanchez

Risk Management

Pharmaceutical Development

Market Strategy

certificate of participation

Receive your certificate of participation

By attending the Genotoxic Impurities Summit 2025, you will receive a Certificate of Participation and a Professional Development Summary outlining your engagement with the latest in impurity control, regulatory updates, and pharmaceutical safety strategies.

+30 000 people

9 years

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