NordInsight helps your team move from finding implant information to reviewing a specific configuration, working through the required checks and documenting the review. With clarity at each stage, there is less to piece together along the way.
Bring structure to the review with curated checklists for screening, day of scan and post-scan. Each phase keeps the relevant checks in view, so your team can follow the process and see what remains.
Mark items as complete, flag anything that needs attention and add notes for your colleagues. Keep questions and observations alongside the checks they relate to.
Give your team a clear overview of progress and outstanding items, helping colleagues understand where the review stands and what needs follow-up.
Export the scan conditions with or without the checklist as PDF or text. For US workflows, continue into a CPT report to build on the work you have already started.
We do the detailed work of organizing manufacturer information into a standardized format, so your team has less to piece together. The Active Implant Module presents the relevant conditions for your selected configuration in a consistent structure that makes the information easier to find, review and use.
Double-checking is built into our quality assurance process. We review the data we present with attention to the details that matter for your assessment. That care gives your team a stronger foundation for reviewing conditions and deciding what needs further attention.
Clear information should be easy to verify. Supporting manufacturer documentation is available alongside the structured conditions, so your team can consult the source, explore the details and bring the information into your local MR safety process.
Every MR safety team deserves access to well-prepared information and practical support. From screening through the day of scan to post-scan, guided checklists help you see what is complete and what remains. Exportable conditions and checklists help you carry that work into your documentation.
A great deal of MR safety work happens outside the manufacturer's stated conditions: off-label scanning, individual risk-benefit analysis, judgment calls made under time pressure. That work is easier to stand behind when the policy that governs it and the escalation path that supports it live in the same system as the review. NordInsight keeps both alongside the conditions and checklists your team is already working through. Read our guide to writing good policies
Not every scan fits the manufacturer's conditions. When a request falls outside them, the decision needs a defined route rather than an ad hoc conversation.
Risk-benefit assessments are part of routine practice. Capturing who reviewed the case, on what basis and what was decided keeps that work defensible.
Your local policy and escalation contacts sit alongside the conditions and checklists, so the next step is visible at the moment it is needed.
Access all supporting documents for each active implant in one folder. Hosted on NordInsight, checked for version accuracy and ready to download.
Every condition comes from the manufacturer's own documentation: the instructions for use, the MR safety sheet, the clinician guide and the radiology guide. We combine them into a single record covering the generator and lead combinations for the system — typically thousands of them — compliant with the manufacturer's guidelines.
For US workflows, you can also start a dedicated CPT report flow with options to add codes 76014, 76015, 76016, 76018 and 76019.
See how the Active Implant Module connects system configuration, scan conditions and documentation in a guided walkthrough.
Implant safety and CPT-ready documentation, in one MRI safety workflow.
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