Save the date for our 2-day international conference on the 4-5th of October in Copenhagen, Denmark. This conference will address biological and clinical evaluations from a risk perspective through a mixture of presentations from standard developers, notified bodies, test houses and device manufacturers. They will present case studies with hands on experience on how to handle different requirements from standards and guidelines.
Who should attend?
This is a must-attend conference for all medical device professionals dealing with biological and/or clinical evaluation, QA/RA Managers, R&D managers, CEO’s. There is something for everyone; both experts in the field and generalists such as decision-makers or senior leading positions.
Stay tuned for more information about the conference and be sure to follow us here or on LinkedIn for the latest updates.
We look forward to meeting you in Copenhagen on the 4-5th of October!
