Anonymous intake by default
Doctors, nurses and admin staff can report patient safety issues or fraud without fear of retaliation. Identity stays anonymous unless the reporter chooses otherwise.

Healthcare workers who report patient safety issues, fraud, or harassment need a confidential channel protected by law. Ashio gives hospital administrators and pharma compliance officers a compliant, anonymous intake that meets EU Directive, member-state health regulations and professional confidentiality rules.
2019/1937
EU Whistleblowing Directive applies to healthcare organisations
50+
Employees — minimum threshold for the directive
7 days
Mandatory acknowledgment deadline
€20/mo
Ashio annual plan, transparent pricing
Overview
Healthcare organisations face unique whistleblower pressures — patient safety, billing fraud, harassment, professional misconduct. Under EU Directive 2019/1937, organisations with 50+ employees must operate a compliant channel. Member-state health laws add duties around medical confidentiality, professional privilege and patient safety reporting. Ashio is designed for these multi-layered obligations.
Regulatory landscape
The whistleblower, safety and ethics stack that healthcare organisations must navigate.
All legal entities with 50+ employees — including hospitals, clinics and pharma — must operate a confidential reporting channel with anonymous intake and strict deadlines.
National health codes (e.g., German SGB V, French Code de la santé publique) impose additional reporting duties around patient safety and professional misconduct.
EU MDR (Medical Device Regulation) requires reporting of incidents and serious events. Ashio handles both whistleblower complaints and device-side incident reports.
Pharma companies face additional requirements from FDA, EMA and national pharmacovigilance rules. Ashio maps to GxP-compliant audit log requirements.
Healthcare fraud is a major EU enforcement priority. Member-state anti-corruption agencies expect effective whistleblower channels.
Why Ashio
Every feature exists because a healthcare compliance team needed it.
Doctors, nurses and admin staff can report patient safety issues or fraud without fear of retaliation. Identity stays anonymous unless the reporter chooses otherwise.
End-to-end encryption means even your IT team cannot read report contents. Only designated compliance staff can decrypt.
One channel for safety reports, fraud, harassment and compliance — with category-based routing to the right team (clinical governance, HR, finance).
Configure per-hospital routing and access controls. National chains, hospital groups and pharma holding companies all work from one Ashio tenant.
Same channel, two destinations. Patient safety reports route to clinical governance; fraud reports to finance; harassment to HR. Configurable per category.
Reports can be categorized on submission and routed to the appropriate team — patient safety to clinical governance, fraud to finance, harassment to HR, medical device concerns to regulatory affairs.
Compliance checklist
Five concerns we hear from hospital administrators and pharma compliance teams — and how Ashio handles each.
Reports are end-to-end encrypted in the reporter's browser. Only your compliance team can decrypt. No PHI exposure, no clinician worry about legal liability.
The report routes to your compliance team, not to the clinical leadership. Access controls on a per-case basis. Anonymous by default. The physician never knows who reported.
Ashio supports both EU Directive whistleblower reports AND MDR device incident reports in the same channel with category-based routing. Set up one intake, multiple destinations.
Auto-recusal. The compliance officer loses access to their own case. A senior designated substitute receives it. The audit log records the recusal — your auditor sees the workflow was followed.
No. Reports are encrypted in the reporter's browser before transmission. IT cannot access content or reporter identity — only designated compliance staff with the right key can decrypt.
FAQ
Yes. Ashio is designed to meet the Directive's requirements: confidential intake, anonymous submission by default, 7-day acknowledgment, and 3-month feedback. Final compliance depends on your own configuration.
Yes. The reporting form works in any modern mobile browser. No app install required.
Only the people you designate as compliance staff, with role-based access controls. IT cannot read report contents or reporter identity.
No. Reports are encrypted in the reporter's browser before transmission. Report contents are not visible to IT, security, or anyone outside your designated compliance staff.
Yes. A 14-day free trial is available, no credit card required.
Related
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