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DANIEL RUBISOIER

Regulatory Affairs Specialist

TÜV SÜD Product Service GmbH

Fließ, Austria

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Regulatory Affairs Specialist at TÜV SÜD with 20+ yrs in medtech. Ensures EU MDR compliance & leads process alignment at TÜV SÜD and also Master Trainer-MDR.

My organisation

TÜV SÜD is a trusted partner of choice for safety, security and sustainability solutions. It specialises in testing, certification and auditing services. Through more than 30,000 employees across over 1,000 locations, the company adds value to customers and partners by enabling market access and managing risks. By anticipating technological developments and facilitating change, TÜV SÜD inspires trust in a physical and digital world to create a safer and more sustainable future.
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About me

Since 2021 at TÜV SÜD

Bevor 15 years experience at several medical device manufacturer

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Speaker sessions (1)

Wednesday, 15 October 2025

15:15 - 16:30

C3: Classification of medical devices

Location:Room 8: Sophie
  • Daniel Rubisoier: Test Your Expertise: Classification of Devices under Regulation (EU) 2017/745 for medical devices

The notified body TÜV Süd agreed to contribute to this session.