MDCG Guidance Published – Appropriate Surveillance Regarding the Transitional Provisions Under Article 120 of the EU MDR MDCG Guidance Published – Appropriate Surveillance Regarding the Transitional Provisions Under Article 120 of the EU MDR The Medical Device Coordination... MDCG Guidance Published – Appropriate Surveillance Regarding the Transitional Provisions Under Article 120 of the EU MDR
IVDR Implementation – Joint Implementation and Preparedness Plan for IVDR Updated IVDR Implementation – Joint Implementation and Preparedness Plan for IVDR Updated The Commission has published an updated version of the... IVDR Implementation – Joint Implementation and Preparedness Plan for IVDR Updated
EFSA ONE Health, Environment, Society – Conference 2022 EFSA ONE Health, Environment, Society – Conference 2022 The EFSA ONE Health, Environment, Society Conference 2022 will... EFSA ONE Health, Environment, Society – Conference 2022
BEIS Webinars on the UKCA Marking and Placing Goods on the Market BEIS Webinars on the UKCA Marking and Placing Goods on the Market The Department for Business, Energy and Industrial Strategy... BEIS Webinars on the UKCA Marking and Placing Goods on the Market
Request for a Preliminary Ruling to the European Court of Justice – Distinction Between Food for Special Medical Purposes, Food Supplements and Medicinal Products Request for a Preliminary Ruling to the European Court of Justice (Case C-760/21) – Distinction between Food for Special Medical... Request for a Preliminary Ruling to the European Court of Justice – Distinction Between Food for Special Medical Purposes, Food Supplements and Medicinal Products
Plastic Packaging Tax – Updates Plastic Packaging Tax – Updates In preparation for the new Plastic Packaging Tax (PPT), which will take effect from 1... Plastic Packaging Tax – Updates
MHRA Guidance Published – Risk-Adapted Approach to Clinical Trials and Risk Assessments MHRA Guidance Published – Risk-Adapted Approach to Clinical Trials and Risk Assessments The MHRA has published guidance on Risk-Adapted Approach... MHRA Guidance Published – Risk-Adapted Approach to Clinical Trials and Risk Assessments
MHRA Guidance Published – Oversight and Monitoring of Investigational Medical Product Trials MHRA Guidance Published – Oversight and Monitoring of Investigational Medical Product Trials The MHRA has published oversight and monitoring of... MHRA Guidance Published – Oversight and Monitoring of Investigational Medical Product Trials
EU Commission – Public Consultation on REACH Regulation Revision EU Commission – Public Consultation on REACH Regulation Revision The European Commission has launched a public consultation... EU Commission – Public Consultation on REACH Regulation Revision
EU Commission Website on Medical Devices from DG SANTE Revamped EU Commission Website on Medical Devices from DG SANTE Revamped The EU Commission’s websites from DG SANTE on medical devices... EU Commission Website on Medical Devices from DG SANTE Revamped
EU Commission Updates the Rolling Plan Containing List of Essential Implementing Acts for the MDR European Commission Updates Rolling Plan The European Commission has updated the Rolling Plan (as of January 2022)... EU Commission Updates the Rolling Plan Containing List of Essential Implementing Acts for the MDR
DEFRA Consultation Outcome – Restriction of Phthalates Medical Devices, Monitoring and Control Instruments DEFRA Consultation Outcome – Restriction of Phthalates Medical Devices, Monitoring and Control Instruments On 14 September 2021 the Department for... DEFRA Consultation Outcome – Restriction of Phthalates Medical Devices, Monitoring and Control Instruments
