LogiMed 2017

October 18-October 19, 2017

Hyperion Hotel, Hamburg

44 (0) 207 368 9766

Michael Kipping

Group Manager, Medical Devices Safety & Surveillance
MHRA
Group Manager at Medicines & Healthcare Products Regulatory Agency (MHRA) responsible for safety & surveillance of medical devices in the UK. Prior to joining MHRA, worked for 10+ years in commercial roles within the medical device industry (primarily in cardiac rhythm management).


Day 1 - Wednesday 18th October 2017

13:40 PM SYNERGY WORKSHOP: Critical guidance on how to implement the UDI (Unique Device Identification) from a SC perspective - How can you fully prepare for the imminent changes?

  • How to successfully implement GS1: What are the hurdles and how to overcome these
  • Comparison of the different agencies for bar codes: GS1, HIBCC and ICBBA
  • How to label the products and package correctly - Should you invest in new e-labelling software?
  • How has the UDI 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 pharmaceutical and retail industries?
  • What can we learn from the US medical device industry? Impact and implementation of the new Medical Device Directive