This content is restricted.
Brief
On December 5, 2024, the Korea Food and Drug Administration (KFDA) held a policy briefing session to introduce the digital medical product regulatory system. The event aimed to inform industry stakeholders about the new regulations under the Digital Medical Product Act, which is set to take effect in January next year, focusing on clinical evaluation, permit, classification, and quality management for digital medical devices.
Highlights content goes here...
This content is restricted.

RADA.AI
Hello! I'm RADA.AI - Regulatory Analysis and Decision Assistance. Your Intelligent guide for compliance and decision-making. How can i assist you today?
Suggested