We are thrilled to announce that the Asphalion team will be attending RAPS Euro Convergence 2025, taking place in Brussels!
Join us in booth #23 to discuss the latest developments in medical devices, IVDs, combination products, and AI.
Want to schedule a meeting with us during the event or need more information? Reach out to us at: [email protected]
We look forward to seeing you there!
Navigating the regulatory pathways for medical device approval in the United States can be complex. Two of the key components in this journey include the Pre-Submission process and 510(k) clearance, both of which engage with the Food and Drug Administration (FDA) to ensure that new or modified devices meet safety standards while supporting innovation and technological progress.
Today, Francisco Rodríguez participated in an engaging roundtable discussion, “Breaking Barriers: Navigating HealthTech Market Access in a Dynamic Landscape,” co-organised by Biocat, BioRegion of Catalonia.
Asphalion te invita a participar en una jornada única, diseñada para profesionales del sector sanitario y farmacéutico que deseen profundizar en los principales desafíos y
Services
SDGs
As a company committed to sustainability, we follow the UN’s 2030 Agenda and its Sustainable Development Goals.
Memberships & PartnershipS
Quality Management System
Innovative SME
SDGs
As a company committed to sustainability, we follow the UN’s 2030 Agenda and its Sustainable Development Goals.
© Asphalion
Schedule here a free 30-minutes meeting with one of our consultants and tell us about your project, challenges or doubts.
We will be happy to assist you!
