About GMIS
MIS was established to close the structural gap between medical technology and real-world healthcare delivery.
Regulatory barriers, fragmented supply chains, and limited technical know-how delay access to life-improving technologies for hospitals and patients.
We pioneer the Integrator Model — an independent, non-manufacturer framework that connects OEM engineering excellence with real-world clinical readiness.
The Integrator Model is led by a senior industry expert with 25+ years in medical technology and end-to-end product execution, supported by a network of collaborators combining OEM insight with regulatory expertise for global market entry.
Our Approach
Three principles guide every engagement we lead.
Execution-First
Our work is measured in deployments, not reports. Every engagement is designed for real-world implementation, regulatory approval, and operational success.
Single-Point Accountability
We lead the full journey — from sourcing decisions to documentation handover — removing coordination burden from OEMs, partners, and clinical teams.
Integration as a Discipline
We treat integration as a core engineering capability, aligning components, workflows, and evidence to support global market entry.