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September 14 @ 14:30 - 17:00

Medicon Valley Alliance have the pleasure to invite you to the 11th meeting within the Medtech Network. The meeting will be hosted by MVA member company Key2Compliance and will focus on Clinical trials in Medtech.  We are looking forward to host a physical event in Copenhagen with insightful presentations followed by networking.

The medical device field is evolving and evidence from clinical investigations is becoming even more important. Device manufacturers are required to both specify and justify the level of clinical evidence needed to demonstrate safety and performance.

As a manufacturer, you will need to consider the clinical development plan as part of your regulatory strategy. A significant question to pose is how to assess the need for clinical investigations and post-market clinical follow-up studies.  While this may be a fairly straight-forward task for new devices more careful considerations are needed for legacy devices.

In this MVA network meeting we will share knowledge on clinical development and important aspects to consider when planning clinical investigations. Examples from device manufacturers will be presented and you will also get an update on the most recent interpretation of MDCG 2020-6 as well as ISO14155:2020.


Date: 14th of September, 2021
Time: 14.30 – 17.00
Host: Key2Compliance
Venue: Medicon Valley Alliance, Auditorium, Arne Jacobsens Alle 15 , 2300 Ørestad City, Copenhagen



14.30 – 15.00
Arrival – registration and networking

15.00 – 15.05
Welcome and introduction by MVA and Key2Compliance 
Petter Hartman, CEO, Medicon Valley Alliance
Åse Ek, Senior consultant and trainer, Key2Compliance

15.05 – 15.10
HØIBERG – European Patent Attorney
Peter Borg Gaarde, Partner, HØIBERG European Patent Attorney

15.10 – 15.30
Setting the scene – the role of clinical data and how to assess the need for clinical investigations
Maria Lindgren, Director Clinical Development, Key2Compliance
Robert Iosif, Team Lead Clinical Development, Key2Compliance

15.30 – 16.00
The newest revision of  ISO 14155 and it’s relation to MDR
Birgitte Berg, Senior Trial Project Manager, Novo Nordisk

16.00 – 16.20
Clinical strategy and clinical development plans – how to adjust to MDR requirements
Sofia Jonhede, Clinical Affairs Director, EU/RoW, Xvivo

16.20 – 16.40
How to build an evidence generation plan for the product life cycle, examples from Stryker
Hanna Schlyter, Senior Director Clinical Affairs, Trauma & Extremities, Stryker

16.40 – 17.00
Questions and discussion

17.00 – 17.30
Deadline for registration is 10th of September, 2021

For more information please contact Sofia Norås sn@mva.org

The Network
MVA Medtech Network gathers the region’s medtech industry to create new partnerships and business opportunities. Joining the network is free of charge for Medicon Valley Alliance members interested in gaining new insights, sharing experiences and networking with like-minded organisations. Non-member organisations and companies are welcome to attend one network event to evaluate membership.


September 14
14:30 - 17:00
View Event Website


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