About the event
DIA Europe 2026, taking place March 24–26 in the dynamic city of Rotterdam, brings together leaders from across the life sciences ecosystem to drive meaningful progress in healthcare. As a premier global forum for regulators, patient representatives, industry innovators, and policy experts, the conference fosters the exchange of diverse perspectives to address today’s most pressing challenges in medicinal-product development.
The conference centers on three pillars — collaboration, innovation, and sustainability — and offers 80+ expert-led sessions across 10 tracks, enabling attendees to explore emerging scientific, regulatory, and market trends shaping the future of global healthcare.
Strategic solutions to launch and manage global products
Cencora provides expert services to plan and execute a successful product launch, combining data, services, and hands-on support to accelerate time to market, reduce risk, and optimize the patient journey. Emerging biopharma companies benefit from a single integrated partnership that scales from local to global markets, while large biopharma companies can rely on global solutions that fill capability and geographic gaps.
Why partner with Cencora?
We offer deep technical expertise, global reach, and strong local market knowledge. By leveraging regulatory pathways specific to each product type, we help streamline approvals and accelerate market access.
Our expertise spans:
- Regulatory Affairs and CMC Requirements
- Patient Safety and Pharmacovigilance
- Market Access Strategy
- Real-world evidence
Join our experts in Rotterdam at the booth H10
Program Management Associate Director, Client Engagement
Navigate Regulatory Complexities With Ease
Regulatory & CMC Services
Bring your product to market faster — with confidence. Our global Regulatory Affairs and CMC experts support you at every stage of development, submission, launch, and lifecycle management. Backed by scientific depth, local‑market insight, and seamless operational delivery, we help you accelerate approvals, stay compliant, and expand globally.
Why partnering with Cencora:
- Faster, smoother launches to get products approved, stay on the market, and grow globally.
- Proactive change management through globally distributed teams with strong local expertise.
- A true extension of your organization, offering flexible regional and local delivery models.
Our core services:
- Health authority advisory
- Regulatory strategy & consulting
- CMC services
- Clinical trial authorization applications
- Marketing authorization applications & procedure management
- Product information & readability services
- Regulatory informatics & operations
- Lifecycle management & post‑approval support
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