Our Process

A five-step pathway from idea to deployment — ensuring compliance, integration, and global readiness.

Five-Step Pathway from Idea to Deployment

This is what it feels like to work with GMIS on a new solution.

1

Discovery & scoping

We begin with a structured discovery session to understand your clinical use cases, target markets, constraints, and success criteria. The outcome is a shared brief and a high-level pathway from today’s state to a deployable solution.

2

Options & feasibility

We scan candidate OEM technologies and architectures, test them against technical, regulatory, and commercial feasibility, and narrow down to a short list of viable options. You receive a clear recommendation and a go / refine / stop decision point.

3

Solution blueprint

Together we define the target solution: which components are used, how they are synthesised, data flows, roles and responsibilities between OEM, GMIS, and local partners, and the phased rollout plan. This becomes the working blueprint for all parties.

4

Build & validation

We coordinate the implementation against the blueprint, while building the evidence, documentation, and training assets needed for regulatory submissions and operational use. The output is a pilot-ready configuration that can be certified and scaled.

5

Launch & continuity

We support initial deployments, onboarding, and workflow integration, and set up the post-market and lifecycle routines that keep the solution safe, compliant, and supportable as you expand to new sites or regions.