Commission proposes targeted simplification of Medical Devices Regulations
New rules aim to ensure better protection of public health while reducing administrative burden for manufacturers, especially small and medium-sized enterprises (SMEs). EU, 16 Dec 2025 — The European Commission has proposed a targeted simplification of the Medical Devices and In Vitro Diagnostic Medical Devices Regulations. The move is designed to address identified shortcomings that […]
MHRA Call for Evidence on AI Regulation Healthcare
UK, 19 DEC 2025 — Understanding MHRA’s Role in AI Regulation for Healthcare the Medicines and Healthcare products Regulatory Agency (MHRA) has formally launched a “Call for Evidence” regarding the regulation of Artificial Intelligence (AI) in healthcare. This initiative supports the work of the newly formed National Commission into the Regulation of AI in Healthcare, […]