EVENT | DIA Europe

DIA Europe 2025 will focus on sustainability, innovation and collaboration – three key pillars for shaping the future of healthcare. From the environmental impact of pharmaceuticals and of the drug development lifecycle to sustainable partnerships and sustainable healthcare systems, DIA Europe 2025 will be the prime opportunity to discuss how collaboration and innovation can support sustainability in healthcare and each stakeholder’s role in making it happen.

DIA Europe 2025 will focus on sustainability, innovation and collaboration – three key pillars for shaping the future of healthcare. From the environmental impact of pharmaceuticals and of the drug development lifecycle to sustainable partnerships and sustainable healthcare systems, DIA Europe 2025 will be the prime opportunity to discuss how collaboration and innovation can support sustainability in healthcare and each stakeholder’s role in making it happen.

February 25, 2025

| ATMPs, Biologicals, Clinical development stage, CMC, Commercialisation & Post-Market, Corporate, EU, Horizon EU Programs, Medical & Scientific Writing, Medical Devices, Preclinical development stage, Procedures, Registration, Regulatory Operations: eCTD and Submissions, Upcoming Events

March 18-20 | Congress Center, Basel

Our experts Núria Romero, Lidia Cánovas, Blanca Huertas, Kassandra López, Alicia Garrido and Joao Amaral will be available at booth H13 to introduce Asphalion and outline the array of solutions we offer, while also addressing your regulatory requirements in depth.

We also would like to invite you to come by on Wednesday the 13^th for a little surprise from 12 p.m. onwards!!

If you want to schedule a meeting in advance, please contact us at: [email protected]

Looking forward to it!

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ASPHALION will be present at Connection Day 2025

April 16, 2025

We are pleased to announce that ASPHALION will participate in the third edition of Connection Day, organised by Catalonia.Health, which will take place on April

EVENT | eRa conference

April 15, 2025

Join Asphalion and many more Life Science industry experts at EXTEDO’s eRA conference next month in Frankfurt! Our Asphalion team will be exhibiting and speaking

The Pre-Submission Process and the 510(k) Clearance | A Primer for MedTech Innovators

April 14, 2025

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.

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ASPHALION will be present at Connection Day 2025

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The Pre-Submission Process and the 510(k) Clearance | A Primer for MedTech Innovators

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Team

Partners

CSR

AI Ethic Code

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EVENT | DIA Europe

Search

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Related news and events

ASPHALION will be present at Connection Day 2025

EVENT | eRa conference

The Pre-Submission Process and the 510(k) Clearance | A Primer for MedTech Innovators

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