Medical Devices – USA, Europe, Asia and ROW Regulatory News – Jan 2025
USA
Guidance on Premarket Approval Application and Humanitarian Device Exemption Modular Review
The guidance provides information on the Premarket Approval Application (PMA) and Humanitarian...
Device Approval, EU Regulations, FDA, Global Regulations, Healthcare Regulations, Innovation Healthcare, MDR2025, Medical Device, Medical Device Compliance, Medical Device Industry, Regulatory Affairs, Regulatory News, Regulatory Updates