EU MDR – CAMD Published Q&A on Certificates of Free Sale and Article 60 of the MDR EU MDR – CAMD Published Q&A on Certificates of Free Sale and Article 60 of the MDR The Competent Authorities... EU MDR – CAMD Published Q&A on Certificates of Free Sale and Article 60 of the MDR
MHRA Compliance Monitor Overview and Application Process Updated MHRA Compliance Monitor Overview and Application Process Updated From April 2022, MHRA initiated a pilot scheme monitoring companies failing to... MHRA Compliance Monitor Overview and Application Process Updated
MDCG Position Paper on Notice to Manufacturers to Ensure Timely Compliance with MDR Requirements Published MDCG Position Paper on Notice to Manufacturers to Ensure Timely Compliance with MDR Requirements Published The Medical Device Coordination Group... MDCG Position Paper on Notice to Manufacturers to Ensure Timely Compliance with MDR Requirements Published
MDR Implementation – CAMD Statement on EU MDR Transition and Capacity of the Medical Device System Adopted MDR Implementation – CAMD Statement on MDR Transition and Capacity of the Medical Device System Adopted The Competent Authorities for... MDR Implementation – CAMD Statement on EU MDR Transition and Capacity of the Medical Device System Adopted
30th Notified Body has been designated under the EU MDR Germany-based notified body ‘Berlin Cert Prüf- und Zertifizierstelle für Medizinprodukte GmbH’ has been notified as the 30th Notified Body under... 30th Notified Body has been designated under the EU MDR
MHRA Board Meeting – 21 June 2022 MHRA (Medicines and Healthcare products Regulatory Agency) Board Meeting – 21 June 2022 The MHRA Board will meet in public... MHRA Board Meeting – 21 June 2022
Global Self Care Federation Launches Key Highlights on Socio-Economic Value of Self-Care Global Self Care Federation Launches Key Highlights on Socio-Economic Value of Self-Care On 26 May 2022, the Global Self Care... Global Self Care Federation Launches Key Highlights on Socio-Economic Value of Self-Care
EU MDR Implementation – Designation of Notified Bodies EU MDR Implementation – Designation of Notified Bodies The European Commission has published an overview of the applications for designation... EU MDR Implementation – Designation of Notified Bodies
One Substance One Assessment – Public Information Session One Substance One Assessment – Public Information Session The Chemicals Strategy for Sustainability sets the objective to move towards ‘one... One Substance One Assessment – Public Information Session
MDCG March Meeting – Minutes Published MDCG March Meeting – Minutes Published The European Commission has published the minutes from the MDCG meeting... MDCG March Meeting – Minutes Published
UK Approved Bodies for Medical Devices Updated UK Approved Bodies for Medical Devices Updated The SGS United Kingdom Limited Medical Devices Scope document has... UK Approved Bodies for Medical Devices Updated
Team NB Press Release and Data Presentation on 2021 Annual Sector Survey Team NB Press Release and Data Presentation on 2021 Annual Sector Survey Team NB has published a press release and... Team NB Press Release and Data Presentation on 2021 Annual Sector Survey
