As a part of the targeted activities for manufacturing industry, Business Finland's Smart Life Finland program together with RaLex Partners is organizing a public webinar training on how to turn the EU Medical Device (MDR) and In Vitro Medical Device (IVDR) Regulations from a regulatory trade barrier to a competitive edge for Finnish companies. The webinar is a continuation for the publication of the EU MDR & IVDR booklet.
Come and join the webinar to learn the latest developments on regulations from the experts! The webinar will be arranged on September 17th at 9.30-16.30.
Agenda
9.30.11.30 How to cope with obstacles when the medical device is ready to be manufactured, sold and marketed?
Tom Ståhlberg, RaLex Partners
11.30-12.30 Break
12.30-14.30 How to cope with obstacles when developing a medical device?
Tom Ståhlberg, RaLex Partners
14.30-15.00 Break
15.00-16.00 AHMED: Agile and Holistic MEdical software Development Co-Innovation Project
Jari Ahola, Smart Health Research Team Leader, VTT
- ML/AI challenges in regulated context
Antti Siipola, Senior Project Manager, Bittium Oyj - Solita Health RegOPS
Kimmo Kivirauma, Business Director, Solita Oy - From documentation burden to agile advantage
Pasi Ahola, CEO & Founder, Taipuva Consulting
16.00-16.20 Aiforia's success story of developing a medical device including artificial intelligence
Juuso Juhila, Director of Clinical Products at Aiforia Technologies
16.20-16.30 Q&A and conclusions
Tom Ståhlberg, RaLex Partners
Webinar material:
Part 1:MD competitive edge post-market
Part 2: MD- competitive edge pre-market
AHMED: Agile and Holistic MEdical software Development Co-Innovation Project
