RegTalk – December 2025 | Global MedTech Regulatory Updates скачать в хорошем качестве

RegTalk – December 2025 | Global MedTech Regulatory Updates

Stay Ahead in MedTech | Global Regulatory Trends That Shaped 2025 In this RegTalk recap, we summarize the most consistent regulatory trends impacting medical devices and IVDs worldwide throughout 2025, based on insights from 11 monthly global regulatory webinars. Rather than isolated changes, this year showed clear patterns across regions — pointing to where regulation is heading next. What Defined Global Regulation in 2025: Digitalization of Regulatory Systems Regulators accelerated the shift to fully digital submissions and lifecycle management. Examples include Pakistan’s complete move away from manual submissions, expanded e-portals in Botswana and Serbia, and increasingly structured digital guidance in Singapore and Malaysia. Greater Transparency & Documentation Control Authorities reinforced clearer records, public-facing documentation, and stronger Authorized Representative accountability. Russia and Oman led this trend by tightening dossier maintenance and making operational information publicly accessible. Stronger Control of High-Risk Technologies & Traceability Labeling and traceability requirements expanded significantly, with broader UDI adoption and IMDRF alignment. Egypt introduced one of the largest labeling overhauls of the year, while Australia released one of the most structured global UDI timelines. AI & Digital Medical Products Regulation 2025 marked a turning point for AI governance. South Africa issued continent-leading AI guidance, while South Korea introduced a full legal framework for digital medical technologies, including software lifecycle and version control. Modernized Registration & Renewal Frameworks Many countries extended registration validity, moved renewals fully online, and simplified processes. The Philippines, Serbia, Botswana, and Oman all introduced frameworks aimed at long-term efficiency and scalability. Updated Device Classification Rules Classification systems evolved to reflect new technologies and risk profiles. China, India, and Mercosur updated rules to better address digital therapies, implants, and emerging technologies. Expansion of Reliance Mechanisms Reliance pathways accelerated approvals without compromising safety. Kenya and South Korea stood out with expanded reliance and fast-track programs to support innovation and market access. Reinforced QMS & Self-Inspection Expectations Authorities raised expectations around internal controls, audits, and ISO 13485 compliance — particularly in China and South Africa. Extended Transition Periods Recognizing implementation complexity, several regulators extended compliance timelines, including Russia and the UAE. The Big Picture: 2025 was a year of regulatory modernization. Digital systems, traceability, AI oversight, and IMDRF alignment are no longer optional — they are becoming the global standard for market access. Stay informed. Stay compliant. Stay ahead. For more regulatory intelligence and global market access support, visit: www.arazygroup.com #RegTalk #ArazyGroup #MedicalDevices #IVDs #MedTech #RegulatoryTrends #GlobalRegulatory #Compliance #MarketAccess #DigitalHealth #UDI #IMDRF