Italy’s New Guidelines on the Advertising of Medical Devices, IVDs, and Surgical Medical Devices Posted on August 19, 2025August 20, 2025 by regdeskmwd
Regulatory Compliance for SaMD: A Practical Guide for MedTech Teams Posted on August 18, 2025September 3, 2025 by regdeskmwd
Nigeria Proposes New Medical Device & IVD Regulation: What MedTech Teams Need to Know Posted on August 14, 2025August 21, 2025 by regdeskmwd
Never Miss a Change: Smarter Regulatory Alerts for MedTech Teams Posted on August 13, 2025August 14, 2025 by regdeskmwd
Kyrgyzstan Issues Transitional Amendments to Support Seamless Shift to EAEU Regulatory Framework Posted on August 7, 2025August 15, 2025 by regdeskmwd
MedTech Regulatory Submissions: The Power of Automation Posted on August 6, 2025August 14, 2025 by regdeskmwd
South Korea’s Updated MFDS Pre-Consultation Guideline: What Medical Innovators Need to Know Posted on July 30, 2025August 14, 2025 by regdeskmwd
The FDA vs. EU AI Act: What Regulatory Teams Must Know Now Posted on July 28, 2025September 3, 2025 by regdeskmwd
Guidelines for the Conduct and Reporting of Good Clinical Practice Inspections Posted on July 24, 2025September 8, 2025 by regdeskmwd
