What Medcxy is, and what it runs on

What we do

Marketing, compliance and clinical teams in aesthetics work across regulations, platform rules, product registrations and clinical literature. Medcxy breaks a request into steps, retrieves from those sources, and returns an answer with citations — so the team can check the reasoning instead of trusting a black box.

What the platform covers

• Compliance review across 7 jurisdictions: mainland China, US, UK, EU, Australia, Japan, South Korea
• Product registration data wired to four official registries: NMPA (China), EUDAMED (EU), MFDS (South Korea) and PMDA (Japan)
• Clinical evidence search over public literature sources, with references kept alongside the answer
• A model committee for high-stakes questions: several models cross-check, and disagreements are shown rather than flattened

How our content is produced

Blog articles are written by the Medcxy data and compliance teams from public regulations and registry sources, and revisited when those rules change. We don't publish invented case studies, and we don't claim certifications or credentials we don't hold.