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IVDR, MDR

National language requirements in the EU for MDR & IVDR devices

The European Commission has released a table on the existing language requirements for manufacturers under MDR and IVDR, compiling all national language requirements required for…

January 18, 2024
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Pablo De Mingo Monge 2024-01-18T10:25:57+01:00
IVDR

IVDR Joint Implementation Plan has been published!

The Medical Devices Coordination Group (MDCG) has issued a joint implementation and preparedness plan for the In Vitro Diagnostic Medical Devices Regulation (IVDR). This plan…

January 16, 2024
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Pablo De Mingo Monge 2024-01-16T09:59:42+01:00
IVDR, MDR

Regulatory updates: January 2024

With the start of 2024, the EU, UK, and Swiss competent authorities provided new regulatory documents. In this post, we will provide an overview of…

January 12, 2024
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Pablo De Mingo Monge 2024-01-12T14:25:44+01:00
MDR

MDR: 43rd Notified Body on NANDO!

The NANDO database has a new Notified Body under the MDR! CESKY METROLOGICKY INSTITUT a. s. is the 43rd EU Notified Body notified under the…

December 21, 2023
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Webmasters 2023-12-21T12:24:03+01:00
IVDR, MDR

Business associations’ letter on EUDAMED mandatory use

Six industry associations on medical devices and healthcare have jointly signed an open letter on the mandatory use of EUDAMED. The six associations call for…

December 19, 2023
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Simona Varrella 2023-12-19T13:40:56+01:00
IVDR

MedTech Europe’s recommendations on May 2025 deadline for Class D IVDs

MedTech Europe published a new position paper ahead of May 2025 deadline for Class D IVDs. These are IVD devices of the highest risk-class. They…

December 18, 2023
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Simona Varrella 2023-12-18T17:16:35+01:00
IVDR, MDR

New Team-NB position paper on medical device lifetime

Team-NB has released a document to clarify the concept of “medical device lifetime”. The Medical Devices Regulation (MDR) does not specifically provide a definition for…

December 18, 2023
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Pablo De Mingo Monge 2023-12-18T11:22:09+01:00
MDR

First MDCG Guidance documents on Annex XVI products

In December 2023, the Medical Device Coordination Group (MDCG) published for the first time two guidance documents on Annex XVI devices. Annex XVI products are…

December 14, 2023
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Simona Varrella 2023-12-14T14:59:03+01:00
MDR

Updated MDCG Guidance on clinical investigation

A clinical investigation can demonstrate a medical device’s safety and clinical performance. In December 2023, the Medical Device Coordination Group updated the guidance on clinical…

December 12, 2023
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Simona Varrella 2023-12-12T15:59:53+01:00
IVDR

First EU Reference Laboratories designated under the IVDR!

The European Union designated on 5 December 2023 its first EU reference laboratories (EURL) for vitro diagnostic devices. In July 2022, the European Commission opened…

December 6, 2023
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Pablo De Mingo Monge 2023-12-06T15:46:11+01:00
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