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NeuroLTC

FAQ

Questions we actually get

Straight answers, including about what NeuroLTC is not. Anything missing? Email us.

Which EHRs does NeuroLTC work with?
NeuroLTC integrates with PointClickCare first, via its FHIR API. The integration is read-only by design — we read medications, conditions, and demographics to build the compliance picture; we never write to the chart. Facilities on other EHRs can start with our CSV import wizard while we expand integrations.
Is NeuroLTC a clinical decision support tool?
No. NeuroLTC is a documentation support and compliance tracking platform. It is not a clinical decision support system, does not provide medical advice, and does not replace clinical judgment or professional psychiatric services. It tells you where the documentation thread is incomplete — what to prescribe is never its business.
How do you handle PHI? Do you sign a BAA?
We execute a Business Associate Agreement with every facility customer before any protected health information is processed. Until a BAA is in place, pilots can run entirely on synthetic demo data — a first-class mode of the product, not a stripped-down sandbox.
How long does a pilot run?
Typically 60–90 days. We scope it with you up front: which units, which measures (GDR currency, PRN stop dates, consent completeness, survey-packet turnaround), and what success looks like. You can start on demo data and connect real data mid-pilot once the BAA is signed.
How is NeuroLTC priced?
Per certified bed, per month, tiered by facility size. We quote it plainly before a pilot starts — contact us with your bed count and we'll send the number, not a sales sequence.
How long does implementation take?
Days, not months. There is no new charting system to roll out: connect PointClickCare read-only or import a census CSV, map your units, and the compliance rules start running. Staff training is measured in a single in-service, because staff keep working in the EHR they already know.
Does this replace our consultant pharmacist?
It complements, not replaces. The consultant pharmacist's monthly review is the regulatory minimum — NeuroLTC covers the weeks in between, flagging lapsed PRN stop dates, due GDR attempts, and missing consents continuously so the monthly review starts from a clean queue instead of a cold chart audit.
Where does AI fit in — and where doesn't it?
Every automated check is a documented compliance rule mapped to a specific F-tag — auditable, versioned logic, not a black box. Where AI drafts a trend summary, it is clearly marked as a draft and a staff member must explicitly review and acknowledge it. AI inputs are PHI-minimized: internal identifiers, never resident names.
What is your security posture?
Access is facility-scoped and role-based, every data path is authorized at the function level, and every access and change is written to an audit log. Our architecture is HIPAA-minded from the ground up. SOC 2 Type II is on our roadmap — and until it's complete you won't see a badge for it on our site.
Who at the facility actually uses it?
Directors of Nursing and administrators use the Compliance and Reports modules most; providers and psychiatric teams live in Rounds and Insight; consultant pharmacists use Monitor. The family portal shows appropriately limited, purpose-scoped information to authorized family members.

Ready to see it against your own survey calendar? Request pilot access.