Commission Announces Action for Safe and Sustainable e-Commerce Imports The Commission is taking action to tackle risks stemming from low-value imports sold via non-EU online retailers and marketplaces hosting non-EU traders. These actions are part of the Communication on E-Commerce, ‘A Comprehensive EU Toolbox for Safe and Sustainable E-commerce', which the Commission is proposing. Commission Announces Action for Safe and Sustainable e-Commerce Imports
CMDh Report – January 2025 Meeting The Co-ordination group for Mutual recognition and Decentralised procedures – human (CMDh) has published the report from the meeting held on 28-30 January 2025. CMDh Report – January 2025 Meeting
European Health Data Space Webinars The EU Health Policy Team of the European Commission is hosting a series of webinars on the European Health Data Space. European Health Data Space Webinars
UK ePI Task Force Update The UK ePI Task Force is co-led by PAGB, ABPI and BGMA and is working for user-centred, digital-first medicines information. An update from the Task Force has been shared. UK ePI Task Force Update
EMA – Questions & Answers on Article 117 – Fifth Revision Published EMA has updated its guidance on the implementation of EU regulations on medical devices and in vitro diagnostic medical devices to address situations when a declaration of conformity is not available for class I integral medical devices. EMA – Questions & Answers on Article 117 – Fifth Revision Published
AESGP Webinar – Interruption or Discontinuation of Supply Under Article 10a MDR: Practical Guidance On 27 February, AESGP is hosting a webinar on the interruption or discontinuation of supply under Article 10a MDR. AESGP Webinar – Interruption or Discontinuation of Supply Under Article 10a MDR: Practical Guidance
UK-wide Licensing for Human Medicines: Supplementary Guidance Published MHRA has published supplementary information on the licensing of medicines for human use in the UK following the agreement of the Windsor Framework. UK-wide Licensing for Human Medicines: Supplementary Guidance Published
HPRA – Guide to Labels and Leaflets of Human Medicines The Health Products Regulatory Authority (HPRA) has published an updated guide to labels and leaflets of human medicines. HPRA – Guide to Labels and Leaflets of Human Medicines
European Shortages Monitoring Platform Fully Live The European Shortages Monitoring Platform (ESMP) has now gone fully live. MAHs can now log in and begin using the platform. European Shortages Monitoring Platform Fully Live
EMA Publishes Final Guideline on Specific Adverse Reaction Follow-Up Questionnaires (Specific AR FUQs) EMA has released the final guideline on Specific Adverse Reaction Follow-Up Questionnaires (Specific AR FUQs). EMA Publishes Final Guideline on Specific Adverse Reaction Follow-Up Questionnaires (Specific AR FUQs)
MHRA Engagement on Facilitating the Use of Digital Packing Notes to Accompany Medicinal Products MHRA is seeking views from stakeholders to understand potential impacts and benefits of a proposal to facilitate the use of digital packing notes to accompany medicinal products. MHRA Engagement on Facilitating the Use of Digital Packing Notes to Accompany Medicinal Products
PackUK Launched: the Scheme Administrator for Packaging Extended Producer Responsibility PackUK will implement the UK’s new Extended Producer Responsibility for packaging (pEPR) programme. The EPR SI came into force on 1 January. PackUK Launched: the Scheme Administrator for Packaging Extended Producer Responsibility
