Operational Compliance & Global Logistics of POC Devices

Partner with qointa for Confidence in Compliance

With Device360™, you’re not just buying a service — you’re gaining a global compliance partner. We help you reduce risk, accelerate timelines, and protect the integrity of your trial data.

→ Book your compliance readiness assessment today

Provision, track, and manage devices globally — without compliance gaps.

DeviceOps covers the end-to-end operational chain for POC devices, from packaging and labeling to traceability and reuse.

Why it matters:

Logistical non-compliance can cause customs delays, data integrity risks, or patient safety issues — and even regulator escalation.

Our services include:

  • Global logistics & Direct-to-Patient/site provisioning

  • MDR-compliant labeling, customs documentation, UDI management

  • GDP/GSP condition monitoring

  • Importer of Record coordination

  • Reuse & sustainability strategies with 10+ year traceability

Compliance built in:

Operates under ISO 13485, GDP/GSP, EU MDR, FDA 21 CFR, and regional supply chain regulations.

→ Keep your devices moving — compliantly, globally, and on time.