Getting Products Registered in Europe Access to the EU/UK/Swiss Market after the EU MDR/IVDR Implementation

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Access to the EU/UK/Swiss Market after the EU MDR/IVDR Implementation

EUROPE (EU, UK and Switzerland) are major markets for medical devices, rehab and hospital equipment. Regardless whether you’re a South Korean manufacturer of Medical Diagnostics or a Rubber
Glove Manufacturer in Malaysia.

The European Market is market that appreciates quality and a willingness to pay a premium price for its imports. And to exports to Europe by itself is a mark of quality and
international standards.

GETTING YOUR PRODUCTS REGISTERED IN EUROPE is a one- day training session held alongside the 23rd SE-Asian Healthcare Show, Kuala Lumpur from 19 – 21 April 2023. Delegates to the conference will be able to get the latest ‘hands-on’ instructions on how to navigate – the NEW CE Marking” process;
The Brexit (UK requirements) and Swixit (Switzerland requirements) outcome for medical devices will also be discussed.

It goes into details on specific critical subjects for the manufacturer and outlines the changes a manufacturer must consider. This one day training session will ensure that you are kept updated with the latest requirements, and of course un-interupted exports to these vital markets.

With an added bonus of visiting the trade show – in Asia’s best venue – the Kuala Lumpur Convention Centre. A one page summary and sign-up form is available here:

Mr Ludger Moeller
Mr Ludger Moeller, Executive Partner Medical Device Safety Service GmbH (MDSS)
Kuala Lumpur Convention Centre - SE-Asia's most prefered business destination.
Kuala Lumpur Convention Centre – SE-Asia’s most prefered business destination.
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