Asphalion expert Adi Ickowicz will be giving a talk at the technology arena about “The Role of the EU Authorized Representative under the new MDR/IVDR Regulations”.
Do not miss it!
Tuesday, May 23, at 3:00 p.m. local time.
If you want to schedule a meeting in advance, you can send an email at: medtech@asphalion.com. Also, you can contact us by using the event networking platform.
Looking forward to meeting you in Brazil!
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Breaking Regulatory News: European Commission’s Proposal on In Vitro Diagnostic Medical Devices Regulation and EUDAMED Roll-Out
EMA has launched a pilot to give scientific advice on the intended clinical development strategy and proposals for clinical investigation for certain high-risk medical devices.
Article 17 of Regulation (EU) 2017/745 (Medical Device Regulation – MDR) regulates the reprocessing of single-use devices (SUDs) with relevance for the European Economic Area (EEA) which may only take place where permitted by national law and in accordance with this article.
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