Medical Devices and In Vitro Diagnostics Regulations: publication of a consensus statement from the EU Competent Authorities to the EU Commission
Read MoreOn 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 together on the implementation of the MDR & IVDR.
Read MoreThe 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, together with activities focus on the main priorities at this moment and in the near future.
Read MoreThe 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.
Read MoreThe 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 Union.
Read MoreQuestions and Answers on Certificates of Free Sale and Article 60 of Regulation (EU) 2017/745 on medical devices (MDR)
Read MoreIn 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 capacity and system readiness in time for May 2024. The data gathered to date suggest there are multiple causes and no single solution. Finding solutions is a shared responsibility...
Read moreFind out more about CAMD and our ambition for improving medical devices surveillance across Europe...
Read MoreMedical Devices and In Vitro Diagnostics Regulations: publication of a consensus statement from the EU Competent Authorities to the EU Commission
Read MoreOn 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 together on the implementation of the MDR & IVDR.
Read MoreThe 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, together with activities focus on the main priorities at this moment and in the near future.
Read MoreThe 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.
Read MoreThe 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 Union.
Read MoreQuestions and Answers on Certificates of Free Sale and Article 60 of Regulation (EU) 2017/745 on medical devices (MDR)
Read MoreIn 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 capacity and system readiness in time for May 2024. The data gathered to date suggest there are multiple causes and no single solution. Finding solutions is a shared responsibility...
Read moreFind out more about CAMD and our ambition for improving medical devices surveillance across Europe...
Read MoreTwo groups have been set up to help provide clarity on the transition provisions and to facilitate collaboration across the medical devices network, during implementation of the new Regulations.
Read MoreLatest update: All European Competent Authorities (CAs) work together in the Competent Authorities for Medical Devices (CAMD) network to promote patient safety through the consistent development and application of the medical devices regulatory system.
Read More