Update from HMA Core Group: Letter from the HMA Core Group of Medical Devices to the European Commission

By Mina Blaess / On October 23rd, 2024 / In ,

The HMA Core Group for Medical Devices has published a letter emphasizing the readiness of the national authorities responsible for medical devices to collaborate with the European Commission and relevant partners to address the challenges identified within the current regulatory framework. It...

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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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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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Patient safety – the focus for all Competent Authorities for Medical Devices (CAMD) members

By Andrew Queen / On December 10th, 2018 / In , , ,

All European Competent Authorities (CAs) work together in the Competent...

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Joint Action on Market Surveillance of Medical Devices (JAMS) releases progress update

By Andrew Queen / On November 16th, 2018 / In ,

The Joint Action on Market Surveillance of Medical Devices (JAMS) is now two...

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