Korean medical-device SMEs
Standalone software medical devices or hardware teams adding connected software.
Korea paid beta · in preparation
Validate fit, workflow, and boundaries with a limited cohort.
The paid beta is a pre-launch introduction for repeat use with close support. It does not lower security, tenant isolation, or document-integrity requirements.
Companion
Your external QMS remains the official source while product facts, commitments, and working drafts are connected.
Product operations material
Product, regulatory, quality, schedule, and document work—without patient-level PHI or clinical source data.
Introduction sequence
Confirm the data boundary before sending material.
- 01
Organization and product fitConfirm product type, current QMS, and the first use event.
- 02
Contract and data catalogAgree on terms, DPA, allowed material, support, region, and retention.
- 03
Workspace activationSet the organization owner, MFA, and first product baseline.
Start with a fit call
Tell us the organization and product type—not the product files.
The public site does not collect customer content. In email, include only company name, product type, and the workflow of interest.