EUDAMED UPDATE: NEW UNIQUE DEVICE IDENTIFICATION (UDI) DEVICE REGISTRATION v 2.22.0 

WHY THE INDIA-EU FTA IS A GAME-CHANGER FOR MEDICAL DEVICE MANUFACTURERS Europe, 30 Jan 2026 — In a significant step towards improving medical device traceability across the European Union (EU), the European Commission has officially rolled out the EUDAMED user guide for Unique Device Identification v 2.22.0 (UDI) Devices. This new regulation requires manufacturers to […]

INDIA EU TRADE AGREEMENT- UNLOCKING GROWTH AND OPPORTUNITIES FOR INDIA 2047

WHY THE INDIA-EU FTA IS A GAME-CHANGER FOR MEDICAL DEVICE MANUFACTURERS The India EU Free Trade Agreement (FTA) is set to redefine trade dynamics, not just between two major global economic players but also within the medical device sector. As India continues to develop its medical device manufacturing capabilities, this india EU trade agreement provides […]

MHRA GUIDANCE ON DIGITAL MENTAL HEALTH TECHNOLOGIES PUBLISHED

United States, 27 January 2026, The Medicines and Healthcare products Regulatory Agency (MHRA) has formally published new guidance and a suite of online resources focused on the use of digital mental health technologies (DMHT). Developed in partnership with NHS England’s MindEd programme and funded by Wellcome, these resources aim to help the public, clinicians, and […]