EU Commission Website on Medical Devices from DG SANTE IVD Section Added EU Commission Website on Medical Devices from DG SANTE IVD Section Added The EU Commission’s website from DG SANTE on... EU Commission Website on Medical Devices from DG SANTE IVD Section Added
EUDAMED – V2.8 Technical Documentation Updates EUDAMED – Technical Documentation Updates EUDAMED is the IT system developed by the European Commission to implement Regulation (EU) 2017/745... EUDAMED – V2.8 Technical Documentation Updates
EU Commission – FAQ on Medicines and Medical Devices Concerning Sanctions Against Russia EU Commission – FAQ on Medicines and Medical Devices Concerning Sanctions Against Russia The Commission has published “... EU Commission – FAQ on Medicines and Medical Devices Concerning Sanctions Against Russia
32nd Notified Body has been designated under the EU MDR Italy-based notified body ‘BUREAU VERITAS ITALIA S.P.A.` has been notified as the 32nd Notified Body under the EU MDR. The... 32nd Notified Body has been designated under the EU MDR
MHRA Webinar – Changes to Medical Device Adverse Incident Reporting MHRA Webinar – Changes to Medical Device Adverse Incident Reporting Adverse incidents involving medical devices that occur in the UK... MHRA Webinar – Changes to Medical Device Adverse Incident Reporting
EU Commission – 2022 Planned Meetings of MDCG and Subgroups List Updated Commission publishes updated version of 2022 MDCG meetings document On 11 July the European Commission published an updated list of... EU Commission – 2022 Planned Meetings of MDCG and Subgroups List Updated
One Substance One Assessment – Commission Consultation One Substance One Assessment – Commission Consultation The European Commission has launched a second call for evidence concerning a possible... One Substance One Assessment – Commission Consultation
MHRA Publishes 2021 Annual Report of the Human Medicines Regulations 2012 Advisory Bodies MHRA Publishes 2021 Annual Report of the Human Medicines Regulations 2012 Advisory Bodies The Medicines and Healthcare product Regulatory Agency... MHRA Publishes 2021 Annual Report of the Human Medicines Regulations 2012 Advisory Bodies
EUDAMED – Production Release 2.8 EUDAMED – Production Release 2.8 EUDAMED is the IT system developed by the European Commission to implement... EUDAMED – Production Release 2.8
MHRA Annual Report and Accounts 2021 – 2022 Published 0 Share: Share via Facebook... MHRA Annual Report and Accounts 2021 – 2022 Published
MedTech Europe – Final Survey Report MedTech Europe – Final Survey Report MedTech Europe has published their final survey report ‘Analysing the availability of Medical Devices... MedTech Europe – Final Survey Report
EU Commission Updates the Rolling Plan Containing List of Essential Implementing Acts for the EU MDR European Commission Updates Rolling Plan The European Commission has updated the Rolling Plan (as of July 2022)... EU Commission Updates the Rolling Plan Containing List of Essential Implementing Acts for the EU MDR
