EU Medical Device & IVD Regulations Workshop

12 December 2018
Hempsons, 100 Wood Street, London EC2V 7AN
10:30 - 16:00

SEHTA Members £199 + VAT / Non-Members £225 + VAT per delegate.  You will be invoiced by SEHTA via PayPal after you have registered.

Why attend

The new EU Medical Device Regulation (MDR) is in its implementation phase and will be effective from May 2020.  All medical devices will need to comply with this new legislation.  Similarly, the IVD Regulation (IVDR) will be in force from May 2022.  Many companies are not yet ready for the journey let alone have a roadmap of how to get to compliance.

This one-day event will:- 

Provide you with an overview of the key areas likely to need upgrading to comply with the MDR/IVDR

Assist you in assessing your company’s current preparedness for the transition

Give you a clear, practical guide to the next steps that you and your company need to take to gain CE Marking under the MDR/IVDR


Gain an overview of the new EU Medical Device and IVD Regulations

Understand the key areas of compliance required

Understand the technical documentation that should be in place for each device

Gain a plan of action for implementation and CE Marking under the new legislation

Click here for more information and to register your interest.

Book now!