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Get Ahead of AI Regulations – EU AI Act Training

AI is becoming an integral part of our daily lives, and its governance affects everyone, from tech giants to individual users. Qserve will host a two-day AI Act training in Amsterdam, The Netherlands. Qserve and Industry Experts will explore this pivotal legislation and its implications for the medical device and IVD sectors during this training. Speakers include Gert Bos, Coenraad Davidsdochter,…
Ben Kemp
September 18, 2024
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Action needed now if you use EPO online filing!

Do you use EPO Online Filing (eOLF)? Things are changing on 30 September!  From 1 October 2024, you will no longer be able to renew eOLF Smart Cards that have expired. To continue filing with the IPO via eOLF, you will need to replace your smart card with a ‘soft certificate’. From 1st January 2025, valid smart cards will no…
Ben Kemp
September 18, 2024
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BSI – Rollout of EU Reference Laboratories for Class D IVDs

As part of BSI Regulatory Services, Medical Devices commitment in maintaining IVDs manufacturers up to date on the EU regulatory framework developments, we issue this communication in regard of the rollout of EU Reference Laboratories and oversight of Class D IVDs in Europe. On 5 December 2023, five EU reference laboratories (EURLs) have been designated through Commission Implementing Regulation (EU)…
Ben Kemp
September 18, 2024