Date(s) - 27/03/2019
9:00 am - 12:00 pm
Understanding MDR’s impact on your supply chain processes
The European Medical Device Regulations 2017/745 (MDR) was published May 5, 2017 in the Official Journal of the European Union, replacing current MDD and AIMDD regulations. Although full implementation is far in the future (2020) early action s required, as MDR will have major impact on all economic operators in MD&D’s supply chain networks. Given the complexity of these new regulations, economic operators should define transition strategies depending on several factors. Extensive and detailed planning will therefore be key in the successful deployment of these strategies.
Although the new MDR looks very QA/AR related (e.g. Post Market Surveillance, QMS changes, integration with EUDAMED databases) the impact on supply chain planning should not be underestimated and this subject should be very high on your priority list. Probably you and your team are already involved in defining transition strategies for dealing with this, but to make the impact of MDR even more transparent we invite you to this special event to share knowledge around this theme.
Details of the event
|March 27, 2019 – 09.00 – 12.00 hrs|
|Participation is free-of-charge and on invite only. However please contact us, if you know people that are also interested in attending.|