54th CAMD meeting statement

By Mina Blaess / On May 22nd, 2024 / In

On 14-15 March 2024, the Belgian Presidency of the Council of the European Union held the 54th meeting of the EU Competent Authorities for Medical Devices (CAMD) in Ghent, Belgium. The meeting covered topics such as ongoing market surveillance activities, emerging challenges and the work done...

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53rd CAMD meeting statement

By Caroline CHIUMIA / On November 20th, 2023 / In

The Spanish Presidency of the Council of the European Union held the 53rd meeting of the EU Competent Authorities for Medical Devices (CAMD) on the 19-20 of September 2023, in Santiago de Compostela, Spain. The agenda for this meeting was a continuation of the work done under previous presidencies,...

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52nd CAMD meeting statement

By Caroline CHIUMIA / On July 11th, 2023 / In

The European Competent Authorities for Medical Devices (CAMD) met for its 52nd meeting in Uppsala, Sweden on the 1st – 2nd June 2023 under the Swedish Presidency of the Council of the European Union. The CAMD meeting in Sweden was dedicated to some of the major challenges we are facing in the...

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51th CAMD meeting Statement

By Camd Admin / On November 24th, 2022 / In

The European Competent Authorities for Medical Devices (CAMD) met for its 51st meeting in Prague on the 20th – 21st October 2022 under the Czech Presidency of the Council of the European...

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Questions and Answers on Certificates of Free Sale and Article 60 of Regulation (EU) 2017/745 on medical devices (MDR)

By Camd Admin / On June 16th, 2022 / In ,

This Questions and Answers document was developed by competent authorities, with the aim of providing guidance in the area of Certificates of Free Sale. It considers how certificates of free sale should be processed/ generated for ‘old’, ‘legacy’ and MDR compliant devices. It highlights...

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CAMD Statement – 50th CAMD Plenary meeting

By Camd Admin / On June 10th, 2022 / In , ,

In the context of the French Presidency of the EU Council, during its 50th plenary meeting, CAMD adopted a statement, following discussions about transition to MDR and capacity of the medical device system. CAMD recognise the significant and urgent challenges that remain in ensuring sufficient...

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MDR, 2021 may 26th, Date of Application is now !

By Virginie GAIFFE / On May 25th, 2021 / In , , ,

The 26th May 2021 marks the full application of the new EU Regulation on...

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The JAMS layman’s report is now available online!

By Lara Laine-Lemarchand / On May 20th, 2021 / In ,

The Joint Action on Market Surveillance of medical devices (JAMS) was set up to...

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JAMS Stakeholder Conference Held In Brussels On Dec. 12th 2019

By Lara Laine-Lemarchand / On January 8th, 2020 / In , ,

Officially launched on October 2019 at the 39th meeting of the Competent...

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EUDAMED State of play : Open letter from the CAMD Executive Group

By Lara Laine-Lemarchand / On November 28th, 2019 / In ,

Following the public announcement by the European Commission of the...

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