MHRA Webinar Recording- Medical Devices Regulations – Tuesday 24 January 2023 MHRA Webinar Recording – Medical Devices Regulations – Tuesday 24 January 2023 On 24 January MHRA hosted a Medical Devices... MHRA Webinar Recording- Medical Devices Regulations – Tuesday 24 January 2023
EU MDCG 2023-3 Questions and Answers on Vigilance Terms and Concepts EU MDCG 2023-3 Questions and Answers on Vigilance Terms and Concepts The Commission has published a new document:... EU MDCG 2023-3 Questions and Answers on Vigilance Terms and Concepts
EU Commission – CLP Revision – Public Consultation Deadline Extended EU Commission – CLP Revision – Public Consultation Deadline Extended In December 2022 the European Commission published its proposal for... EU Commission – CLP Revision – Public Consultation Deadline Extended
MHRA Consultation on Proposals to Increase Statutory Fees – Government Response MHRA Consultation on Proposals to Increase Statutory Fees – Government Response The government response to consultation on proposals for changes... MHRA Consultation on Proposals to Increase Statutory Fees – Government Response
Government Response to Regulatory Horizons Council Medical Device Report Government Response to Regulatory Horizons Council Medical Device Report The Regulatory Horizons Council (RHC) published a report containing recommendations on... Government Response to Regulatory Horizons Council Medical Device Report
MDR Implementation – Coverage of Designation Codes by NBs MDR Implementation – Coverage of Designation Codes by NBs The European Commission has published an updated summary on coverage of... MDR Implementation – Coverage of Designation Codes by NBs
Chair of MHRA’s Interim Devices Working Group Appointed Chair of MHRA’s Interim Devices Working Group A... Chair of MHRA’s Interim Devices Working Group Appointed
European Commission Proposal on Packaging and Packaging Waste – Public Consultation – Deadline Extension European Commission Proposal on Packaging and Packaging Waste – Public Consultation – Deadline Extension The European Commission’s... European Commission Proposal on Packaging and Packaging Waste – Public Consultation – Deadline Extension
37th Notified Body has been designated under the EU MDR Germany-based notified body ‘SLG PRÜF UND ZERTIFIZIERUNGS GMBH’ has been notified as the 37th Notified Body under the MDR The... 37th Notified Body has been designated under the EU MDR
MDCG Guidance – List of Standard Fees MDCG Guidance – List of Standard Fees The Commission has published the MDCG Guidance 2023-2 List of standard fees.Article 50... MDCG Guidance – List of Standard Fees
MHRA Webinar – Medical Devices Regulations – Tuesday 24 January 2023 MHRA Webinar – Medical Devices Regulations – Tuesday 24 January 2023 MHRA is hosting a Medical Devices Regulations webinar, which... MHRA Webinar – Medical Devices Regulations – Tuesday 24 January 2023
MDR/IVDR Implementation – Legislative Proposal to Amend Transitional Provisions Published MDR/IVDR Implementation – Legislative Proposal to Amend Transitional Provisions Published The Commission has adopted a legislative proposal to amend the... MDR/IVDR Implementation – Legislative Proposal to Amend Transitional Provisions Published
