MedEQ is an AI-powered continuing education platform built for healthcare practitioners who want to stay current with the latest FDA drug approvals and medical device clearances, without sacrificing a week of practice for a conference.
The FDA approves roughly 50 major drugs and over 3,000 medical devices per year. Most practitioners learn about these through multi-day conferences that pull them away from patients, or through a system of continuing education that hasn't fundamentally changed in decades. The typical experience: fly to a resort, sit through morning lectures, take an easy test with a 60% pass rate, and collect your credits. The education doesn't stick, and patients suffer when their providers aren't current.
At the same time, tools like Open Evidence have tried to put medical knowledge at practitioners' fingertips, but accuracy issues remain a concern in high-stakes clinical settings.
MedEQ takes a different approach. We deliver micro-learning modules, each focused on a single new drug or device approval, that practitioners can complete during their daily commute or between patients. Each module consists of:
MedEQ is currently in MVP development. We are pursuing accreditation through ACCME (Accreditation Council for Continuing Medical Education) partnership. CE credits shown on this platform are pending formal accreditation and are for demonstration purposes during the MVP phase.
This platform is currently in development and demonstration phase. Clinical content has been reviewed but CE credits are not yet formally accredited. Content is based on FDA-approved prescribing information and peer-reviewed literature.
For questions about MedEQ, partnership inquiries, or clinical content feedback, please reach out to our team.