-659d2d07.webp)
MRI safety, connected
NordInsight brings manufacturer evidence, scanner conditions, local guidance, and approvals into one connected workflow, helping MRI teams make consistent decisions with a clear record of how each decision was reached.
Used every day by thousands of MRI professionals.
The difficult part is determining whether you have the right device, understanding which conditions apply to the available scanner, incorporating your department’s guidance, and documenting the final decision.
When those steps happen across PDFs, shared drives, inboxes, and individual experience, important context becomes disconnected. NordInsight brings the complete decision into one workflow.
Identification can begin with incomplete or inconsistent information.
Manufacturer evidence must be weighed against the scanner and local guidance.
The source, assessment, approval, and outcome need to remain traceable.
The connected workflow
Each step builds on the same source-backed record, so the information gathered during research stays connected to the assessment, the local decision, and the final documentation.
Identify
Search by device type, manufacturer, model, or partial identifying information. NordInsight helps the team move from an incomplete description to the most relevant record without navigating scattered folders and documents.
Review
See device details, structured MRI conditions, warnings, source documentation, and review history in one clear record, giving your team the context needed before moving to a decision.
Understand
Review structured manufacturer conditions alongside the scanner being used and the guidance your department has approved. Critical warnings and limitations stay connected to their original source.
Document
Capture the source, assessment, local context, and approval in one traceable record. The resulting summary can support the patient pathway, departmental governance, and reporting.
Capture the information needed to support CPT reporting within the same documented workflow, helping teams connect the clinical assessment with the relevant reporting requirements.
We’ll focus the conversation on your scanners, policies, and decision process.
Policies and escalation
Bring department policies, review dates, owners, and escalation contacts into the same trusted workspace as your implant information.
Give the team fast access to current policies, supporting documents, and department procedures without searching across shared drives and folders.
Connect each policy to the appropriate contact or responsible person, helping staff understand when and where to escalate a question.
Trust & validation
NordInsight is designed to help MRI teams understand where information came from, when it was reviewed, and how it contributed to the final decision.
01
Original IFU
02
Last reviewed
03
Local guidance
04
Decision history
Every record is checked by a qualified reviewer before it reaches your team.
Every claim links back to the original manufacturer document, not a summary of a summary.
See exactly when a record was last checked and by whom, at a glance.
Escalations and local policy decisions stay tied to the record that prompted them.
The platform
NordInsight connects the information, people, and departmental processes surrounding an MRI safety decision — configured around the way your team works.
Bring device identification, required information, and escalation into a clearer, documented pathway.
Review limitations in the context of the scanner and room the patient will actually use.
Keep local guidance, owners, review dates, and escalation contacts connected to the decisions they support.
Preserve a structured trail from source evidence to local assessment, approval, and outcome.
There's more behind each workflow than we can show on one page.
See the platform in a demo.webp)
For your department
Give the team the same sources, local guidance, and documented decisions instead of relying on individual memory or separate folders.
Bring the relevant record, manufacturer evidence, scanner context, and department guidance into one connected view.
Maintain ownership, review history, and a traceable record of how local decisions were reached.
Support
Every user gets direct access to people who understand both the platform and the realities of MRI safety practice.
4.9/5
Support rating
~1 min
Average response time
“
MRI safety questions rarely fit neatly into a template. Teams need support from people who understand the clinical context and can help them work through the details.
Kellye Chia, RT(R)(MR), MRSO(MRSC), MRSE(MRSC)
Director of Clinical Success and MRI Safety, NordInsight
In a tailored demo, we'll show how NordInsight connects manufacturer evidence, scanner conditions, local guidance, and documentation around the way your department works.
FAQ
Is NordInsight only an implant database?
No. Implant research is one part of a connected platform that also brings together scanner information, local policies, approvals, documentation, reporting, and departmental resources.
Is the information connected to the original manufacturer source?
Yes. Manufacturer documentation is attached to the relevant implant record, allowing teams to review the source behind the structured MRI conditions.
How are implant records reviewed and maintained?
Implant conditions are read from manufacturer documentation and checked by trained reviewers before publication. Source versions, review dates, and change history help teams understand when and how the information was reviewed.
Can we include our department's policies and guidance?
Yes. Local policies, notes, supporting documents, owners, and escalation contacts can be kept alongside the implant information they support.
Can NordInsight reflect our scanners and MRI rooms?
Yes. Scanner and room information can be maintained in NordInsight, helping teams consider implant conditions in the context of the equipment being used.
Does NordInsight support active implant workflows?
NordInsight supports structured workflows for active implants, including pacemakers and neurostimulators, helping teams keep identification, requirements, escalation, and documentation connected.
Can we document local decisions and approvals?
Yes. Local notes, approvals, supporting guidance, and the people involved can be recorded alongside the relevant implant record, creating a traceable history of the decision.
Does NordInsight support CPT reporting?
For US hospitals, NordInsight can help capture the information needed to support CPT reporting within the same documented workflow.
What support do users receive?
Every user gets direct access to the NordInsight support team. Questions are handled by real people who understand the platform, with a current support rating of 4.9 out of 5 and an average response time of approximately one minute.
What does implementation look like?
Implementation is shaped around your department, including your scanners, policies, responsibilities, and existing ways of working. We can discuss setup, onboarding, and rollout during the demo.
What will you show us in a demo?
We will walk through the workflow from implant identification to a documented decision and focus on how NordInsight could fit your department's scanners, policies, and responsibilities.
Implant safety and CPT-ready documentation, in one MRI safety workflow.
Get in touch
info@nordinsight.com© 2026 NordInsight · NordInsights Health Tech ApS · 2970 Hørsholm, Denmark · CVR: DK-43001833