CiteMed

Accelerate Regulatory Submissions with AI-Powered Evidence Generation

CiteMed Evidence Cloud streamlines systematic literature reviews for medical device and pharmaceutical regulatory teams. Our platform automates literature screening, data extraction, and compliance reporting—reducing review timelines from weeks to days while maintaining regulatory standards.

Generate FDA and EU-compliant PRISMA reports, conduct post-market surveillance, and perform competitive intelligence analysis through a single, secure platform. With automated workflows and audit-ready documentation, Evidence Cloud eliminates manual processes that delay critical submissions.

Trusted by leading medtech organizations to accelerate time-to-market while ensuring regulatory compliance and evidence quality.