
Veranex Experts at EuroPCR & Innovators Day
Align your clinical, regulatory, and commercialization strategy early and accelerate development.
May 18-22, 2026 | Paris, France
Euro PCR Booth M54
Innovators Day Booth H5
Why Teams Meet Veranex at EuroPCR
Move from innovation to approval with fewer delays, stronger submissions, and a clearer path to market.
Veranex provides coordinated strategy across clinical, regulatory, quality, and commercialization to reduce delays, misalignments, navigate risks. Our approach is grounded in real-world cardiovascular programs and evolving global regulatory expectations.
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700+ experts across clinical, regulatory, quality, and commercialization
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Deep experience across interventional, structural heart, and vascular technologies
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Proven support from early feasibility through global market access
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Integrated model aligning clinical evidence with regulatory and commercial success
Exclusive Sponsor of PCR Innovation Day
18 May 2026 | Paris, France
If you're making decisions that will define your development timeline, this pre-conference event focused on emerging cardiovascular technologies is the right moment to align your strategy.
Connect with us at Innovators Day, to discuss:
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First-in-human readiness and early feasibility strategy
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Clinical evidence planning under MDR and FDA pathways
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Regulatory positioning across EU and US markets
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Key inflection points for funding, trials, and commercialization
See how strategy translates into execution
Located in Paris, Veranex’s PCS preclinical facility supports cardiovascular device development through translational research, procedural simulation, and preclinical testing.
This is where early concepts become clinically and regulatorily viable.
During your visit, you’ll see how our teams integrate:
- Preclinical and translational research
- Clinical study design and execution
- Regulatory and quality strategy
- Commercialization planning
EuroPCR is where critical decisions are made.
The teams that move fastest are the ones that align strategy early.
If you’re evaluating your next clinical, regulatory, or commercialization step, now is the time to have that conversation.



