Protect patient data and every connected device on one living digital twin
Healthcare and MedTech teams have to protect special-category patient data, connected medical devices, and clinical continuity at once. Rizzqo brings every system, device, and supplier that touches patient data into one picture, prices the risk in real money, and keeps the evidence ready at the source, so your teams stay audit-ready instead of scrambling.
Built on the standards healthcare auditors expect
Encrypt a clinical database once and the proof counts three ways: as GDPR security of special-category data, as an ISO 27001 Annex A control, and as a NIS2 Article 21 risk-management measure. One piece of work, three obligations a health-sector auditor checks.
GDPR
Special-category health data handled to the letter: lawful basis, records of processing, breach duties, and patient rights, anchored to the systems that hold the data.
Explore frameworkISO 27001
The security of processing health data demands, evidenced as an ISMS: Annex A controls mapped straight to your clinical systems, devices, and suppliers.
Explore frameworkNIS2
Health is a NIS2 essential sector: hospitals and health and MedTech providers meet the Article 21 risk-management measures and the incident-reporting timeline, mapped to the systems they cover.
Explore frameworkWhat healthcare and MedTech need to handle
Patient data is special-category, devices are connected and long-lived, and the regulatory net keeps tightening. Rizzqo gives you one place to face all of it.
Special-category health data
Patient records sit in the most protected class under GDPR Article 9, so lawful basis, minimisation, and breach duties carry the highest stakes and the highest fines.
Connected medical devices
Infusion pumps, imaging systems, and monitors stay in service for years, often unpatched, each one an asset that has to be inventoried, owned, and risk-assessed.
Sprawling supplier chains
EHR vendors, cloud hosts, labs, and device makers all process patient data. Every processor is a link in your chain and a line in your risk picture.
Tightening regulation
NIS2 and DORA-style resilience duties, MDR, and national health-data rules raise the bar. They are drivers of your program, satisfied through GDPR and ISO 27001 controls.
Clinical continuity
Downtime is not an inconvenience, it is a patient-safety event. Risk has to be priced and reduced where care actually depends on the system.
Audit and certification load
Certification bodies, supervisory authorities, and procurement teams all want evidence. Reconstructing it by hand every time is not sustainable.
What Rizzqo gives healthcare and MedTech teams
Everything that touches patient data, from a connected infusion pump to the evidence an auditor asks for, lives in one place, so your program holds together instead of scattering across spreadsheets.
Inventory every system and device that touches patient data
You can only protect what you can see. Rizzqo brings your clinical applications, databases, connected medical devices, cloud services, and the suppliers behind them into one live picture, so no infusion pump or lab system holding patient data lives in an orphaned spreadsheet.
Price the risk to care in real money
Every system and device carries its own risk. Rizzqo puts a real-money figure on it, say a six-figure exposure behind an EHR outage or a breach of a special-category dataset, not just red, yellow or green. You see where the real loss to patients and the organisation sits, and which fixes actually reduce it.
Map controls to GDPR and ISO requirements
Controls become concrete requirements you can act on, not abstract clauses in a binder: encryption of patient records, access on clinical systems, device segmentation, processor agreements. Segment a device network for patient safety and that single measure counts under GDPR security of processing, your ISO 27001 ISMS, and the NIS2 measures at once, so overlapping obligations are satisfied without redoing the work.
Keep evidence at the source, stay audit-ready
Evidence stays attached where the work happens, and your compliance picture keeps pace as your teams go. So when a supervisory authority opens a breach inquiry on a regulatory clock, the proof for the system in question is already there, and you answer within the deadline rather than chasing clinicians for documents mid-incident.
When a ward goes dark, you already know what is at stake
A ransomware hit on an imaging server, a misrouted patient export, a recalled monitor: in healthcare the question is never just technical, it is which patients are affected and what you owe them by when. Because assets, risk, controls, and evidence live in one place, the answer is already assembled: who is in scope, what it costs, who owns the response. Clinical and security leadership see the same picture, in real money rather than a heat-map colour, and act on it together. Made in Germany, EU-hosted, with your patient data kept on European soil.
Healthcare and MedTech, answered
Rizzqo treats health data as special-category from the start, so the systems that hold it carry the right lawful basis, records of processing, retention, and breach duties. Patient-rights and breach responses are ready against the affected systems, so you respond within regulatory deadlines and can prove it.
Yes. Connected devices are first-class assets, right alongside your clinical applications and suppliers: each infusion pump, imaging system, or monitor is inventoried and risk-assessed, not left off to the side.
Those regulations are drivers of your program rather than separate frameworks here. Rizzqo satisfies their security and data-protection demands through GDPR and ISO 27001 controls, so the work you do counts toward all of them.
Rizzqo prices risk as an illustrative financial exposure, for example the cost of an EHR outage or a breach of a patient dataset, not just a colour on a heat-map. You see where the real loss sits and which fixes actually reduce it, in money.
Rizzqo is Made in Germany and EU-hosted, so your data stays on European soil. That makes it straightforward to evidence data residency and the safeguards your supervisory authority and procurement teams ask about.
Ready to make patient data and devices audit-ready?
See how Rizzqo connects your clinical systems, devices, suppliers, risks, and evidence into one living program, with risk priced in real money and hosted in the EU.