Barcelona Health Innovation Week 2024 | Regulatory tips for IA and software-based Medical technologies

For the second year in a row, Barcelona will celebrate a week devoted to innovation, acceleration, technology and transformation in healthcare, showcasing the diversity, strengths, impact and potential of the thriving life sciences and healthcare ecosystem based in Barcelona. Organised by BioCat, Asphalion will be present again, this time offering a round table workshop at its premises.

For the second year in a row, Barcelona will celebrate a week devoted to innovation, acceleration, technology and transformation in healthcare, showcasing the diversity, strengths, impact and potential of the thriving life sciences and healthcare ecosystem based in Barcelona. Organised by BioCat, Asphalion will be present again, this time offering a round table workshop at its premises.
January 30, 2024

Eager to know how to navigate the dynamic landscape of AI and software-driven medical technologies? Curious about the regulatory challenges in this evolving field? Look no further! We invite you to our insightful workshop where industry experts and innovators gather to share their experiences and insights!

Round Table Discussion: Engage with leading professionals and gain a deeper understanding of the regulatory intricacies surrounding AI in medical technologies.

Diverse Perspectives: Our panel features experts from various domains, ensuring a comprehensive exploration of the challenges and opportunities at the intersection of AI and medical regulations.

Meet our expert panelists:

  • ERNI – Consulting company expert in software development
  • Accexible – Startup developing platform-based on AI models
  • BSI – Notified Body
  • Asphalion – Scientific, Safety and Regulatory Affairs consultancy

 

When? Wednesday 14 February, 2024

Time: 3:00 – 4:30 p.m. CET

Venue: Hotel CAtalonia Barcelona Plaza- Plaza España, 8. 08014 Barcelona

🔗 Register here: Regulatory tips for IA and software based Medical technologies Workshop

 

 

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NEWS | FAQs on the European Health Data Space

The EHDS Regulation has three main parts, each with different addressees:

Chapter II on primary use provides additional rights to patients and establishes the technical infrastructure necessary for their implementation.

Chapter III on Electronic Health Record (EHR) systems is addressed to manufacturers and other economic operators who make EHR systems available on the market.

Chapter IV on secondary use is addressed to health data holders and users.

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