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 Other, Regulatory
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...
Read Full Article51th CAMD meeting Statement
By Camd Admin / On November 24th, 2022 / In Other
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...
Read Full ArticleMDR, 2021 may 26th, Date of Application is now !
By Virginie GAIFFE / On May 25th, 2021 / In Events, Health, Other, Regulatory
The 26th May 2021 marks the full application of the new EU Regulation on...
Read Full ArticlePatient safety – the focus for all Competent Authorities for Medical Devices (CAMD) members
By Andrew Queen / On December 10th, 2018 / In Health, Other, Regulatory, Wellbeing
All European Competent Authorities (CAs) work together in the Competent...
Read Full ArticleJoint Action on Market Surveillance of Medical Devices (JAMS) releases progress update
By Andrew Queen / On November 16th, 2018 / In Other, Regulatory
The Joint Action on Market Surveillance of Medical Devices (JAMS) is now two...
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