Speakers
The Medtech Compliance Forum by Aurevia & RAPS is a dedicated program within Labquality Days, bringing together regulatory and quality professionals, innovators, and medtech leaders to discuss the compliance topics shaping the future of the industry.
Catarina Carrão
Regulatory Clinical Evaluation & Assessment
BioSciPons
Austria
Danielle Giroud
Chief Executive Officer
MD-CLINICALS
Switzerland
Erik Vollebregt
Attorney-at-law/Partner
Axon Lawyers
The Netherlands
Hanna Valo
Fimea
Ilkka Juuso
Lead Auditor, C&T Manager
SGS Fimko (NB 0598)
Finland
Janne West
Senior Quality & Regulatory Affairs Consultant
Aurevia
Sweden
Jari Martelin
Clinical Director
Bittium Medical
Finland
Koen Cobbaert
Regulatory Science & Policy Expert
Philips
Belgium
Krishnadev Moothandassery Ramdevan
Senior Quality and Regulatory Consultant
Aurevia
Sweden
Lassi Rieppo
FIMEA
Mari Levula
SGS
Marika Karjalainen
Quality & Regulatory Affairs Expert
Aurevia
Finland
Mihir Kelshiker
Clinical Scientist
Scarlet
UK
Molly Rogers
Head of IVDR, Medical Europe
DNV
Ireland
Nelli Karhu
Healthtech Finland
Reeta Levo
Bioretec
Reetta Hintsanen
Chief Operating Officer
Gosta Labs
Finland
Rina Wahlroos
VP, Quality and Regulatory Compliance
Aidian
Finland
Surash Surash
Senior Clinical Reviewer
TÜV SÜD
UK