Accelerating Regulatory Submissions: Practical AI Workflows for MDR and IVDR Compliance
Webinar on Accelerating Regulatory Submissions: Practical AI Workflows for MDR and IVDR Compliance Tuesday, November 11 at 11am ET How are medical device and diagnostic manufacturers meeting evolving regulatory standards through AI-enabled systematic literature review workflows? Explore this topic with the experts and gain real-world insights for enhancing transparency, traceability,…