Diana Kanecka

Officer Regulations & Industrial Policy
MedTech Europe, an alliance of EDMA and Eucomed

Diana is responsible for managing the following areas: UDI, Eudamed, Animal By-Products, Software, Environmental groups and the internal market issues. Diana has a strong interest in regulatory topics as well as trade and healthcare policies. She was an active member of the European Health Parliament project where she worked with the 'economic dimension of healthcare' committee on development of the recommendations on the future of healthcare systems.

Check out the incredible speaker line-up to see who will be joining Diana.

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Day 2

Wednesday, October 11th, 2017

16:10 CASE STUDY REVOULTION: Essential guidance from Industry and Eucomed on how to implement the UDI (Unique Device Identification) from the SC perspective - Assess the impact of serialisation on the SC and learn how to minimise disruption

How to successfully implement GS1: What were the hurdles and how were these overcome?
Comparison of the different agencies for bar codes: GS1, HIBCC and ICBBA
How the implementation of UDI affected logistics– what changes had to be made?
How do you label the products and package correctly? Should you invest in new e-labelling software?
How has this helped improve visibility and inventory management?
How to communicate effectively with your regulatory department
Implementation of either printer/label tech on the lines or software infrastructure
What can we learn from the pharma and retail industries?
What can we learn from the US medical device industry?
Maximising the ROI of your UDI implementation, ensuring it continues to drive business value
Impact and implementation of the new Medical Device Directive