Clinical Outsourcing Group (COG) Europe 2025
Let’s connect at COG Europe from November 18–19, 2025, to discuss how our integrated CDMO and CRO solutions, including clinical trial supply services, can help support your research studies.
November 18–19, 2025 | Novotel Amsterdam City, Netherlands | Booth 8
About COG Europe 2025
The 3rd annual COG Europe conference will gather clinical-stage biopharma executives from across the continent to discuss the future of clinical trials and gain insights from leaders in industry, regulation, and academia.
Visit Thermo Fisher Scientific at booth 8 to connect with our drug development experts and explore how our integrated CDMO and CRO solutions, including clinical trial supply services, can support your research studies.
Event details
Date: November 18–19, 2025
Format: In-person
Location: Novotel Amsterdam City, Netherlands
Booth number: 8
Event website: COG Europe | PBC Group
Why Thermo Fisher Scientific?
We provide comprehensive capabilities across drug development, including label design and translation management, strategic comparator and co-medication sourcing, biorepository storage, and distribution and logistics for clinical trials—including for temperature-sensitive products requiring cold, ultracold, and cryogenic conditions.
Whether your investigational drug is a small molecule, large molecule, or advanced therapy, our clinical trial services offer valuable support at every stage of your supply chain—no matter the size or scope of your study.
Schedule a meeting with our experts at COG Europe 2025 to experience the difference of an end-to-end, integrated CDMO and CRO partner. Our unmatched network of industry experts combines the coordination to streamline your supply chain with the diligence to see your study through—helping you get treatments to patients faster.
Attend our keynote session
“Biotech speed, biopharma scale: Powered by clinical trial innovation”
This keynote session will take place on Tuesday, November 18, at 10 a.m. CEST.
The evolving clinical trial landscape demands a delicate balance of reducing waste, ensuring supply chain resilience, and accelerating timelines to meet market demands.
In this session, Antony Davison, senior manager of sales at Thermo Fisher Scientific, will explore key challenges sponsors face in clinical supply management, including minimizing stockout risks, improving shipment visibility, and enhancing efficiency without compromising quality.
Discover how advanced digital enablement tools are transforming supply chain operations, providing real-time insights, and building confidence in supply continuity.
Takeaways will include:
- Strategies to reduce clinical supply waste while meeting patient needs
- Digital tools that enhance real-time shipment visibility and tracking
- Operational innovations to accelerate timelines without increasing risk
- Approaches to aligning supply chain efficiency with clinical trial demands
- Trends such as decentralized clinical trials and direct-to-patient shipping
Find your missing element at booth 8
With 35 years of experience and a global network of 30 purpose-built CGMP facilities, we have the capacity, stability, and expertise to support you from clinical research and manufacturing through clinical supply and execution.
Visit booth 8 to explore our comprehensive capabilities for biotech sponsors.
Alternatively, schedule a 1:1 meeting with our team for an in-depth discussion.
Continuing education for the pharma industry
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We look forward to seeing you soon