Toku
GDPR evidence
Account Receivables Platform for Latin American Enterprises
No public evidenceToku and GDPR
CertReports found no public GDPR evidence for Toku as of unknown date. This does not mean the vendor is non-compliant. It means CertReports found no public evidence at the last check.
Evidence
- Kind
- listing
- Issued or listed
- 8 Jul 2025
- Scope
- Toku collects and processes data through its medical devices and wellness applications primarily to support the following lawful and regulatory-compliant purposes: 1. Provision of Core Health Insights and Services Data is collected to generate clinically validated outputs, including the assessment of health risks (e.g., cardiovascular disease risk through CLAiR, chronic kidney disease risk through MyKidneyAI) or wellness-related indicators (e.g., biological age estimates through BioAge). This processing is necessary for the performance of the services the user or healthcare provider has requested, in accordance with Article 6(1)(b) of the General Data Protection Regulation (GDPR) and the “treatment” or “healthcare operations” provisions under the Health Insurance Portability and Accountability Act (HIPAA). 2. Medical Device Performance and Safety Monitoring Toku collects and monitors usage, output, and performance data to ensure the ongoing safety, effectiveness, and quality of its devices, as required under applicable regulatory frameworks such as the U.S. Food and Drug Administration’s Quality System Regulation (21 CFR Part 820), ISO 13485:2016, and the EU Medical Device Regulation (MDR 2017/745). This includes post-market surveillance, vigilance reporting, and corrective and preventive actions (CAPA) obligations. 3. Research, Validation, and Continuous Product Improvement In compliance with applicable ethical standards and subject to appropriate consent where required (e.g., under GDPR Article 6(1)(a) and 9(2)(a)), Toku may collect de-identified or pseudonymized data to improve device algorithms, validate software updates, conduct clinical studies, and enhance the scientific robustness of its solutions. Such activities are vital for the fulfillment of obligations under the FDA’s Software as a Medical Device (SaMD) guidance and equivalent international standards. 4. Regulatory Compliance and Audit Readiness Data collection ensures compliance with legal obligations under applicable laws and regulations governing medical devices, cybersecurity (such as the FDA’s guidance on cybersecurity in medical devices and ISO/IEC 27001), privacy laws (including GDPR, HIPAA, and New Zealand’s Privacy Act 2020), and audit obligations from notified bodies or regulatory authorities. 5. Security and Integrity of Systems Certain technical and system-related data are collected to maintain the security, confidentiality, and integrity of Toku’s platforms and devices, in accordance with applicable cybersecurity frameworks (e.g., NIST Cybersecurity Framework, ISO/IEC 27001). This supports the protection of patient and user information from unauthorized access, ensuring both regulatory compliance and ethical data stewardship. 6. User Support and Incident Handling Data may also be collected and processed to provide technical support, investigate user complaints, manage recalls, or handle incident reports, pursuant to Toku’s obligations under Good Clinical Practice (GCP), FDA reporting requirements (21 CFR 803, Medical Device Reporting), and MDR vigilance requirements. 7. Anonymization and Aggregated Analytics When permitted under applicable laws and contractual obligations, Toku may use anonymized or aggregated data sets for legitimate business interests, including statistical analysis, public health insights, or operational management. Such processing is performed in accordance with GDPR Recital 26 and equivalent legal standards, ensuring that data subjects are no longer identifiable.
| Source | Captured | Quote | Links |
|---|---|---|---|
Data Privacy Framework list Official registry · HTTP 200 | 17 Sep 2026 | Toku: Inactive | Live pagesha256 2fdd4615d2 |
What GDPR means, and what it does not
"GDPR compliant" is a claim, not a certification. The verifiable facts are a public DPA, SCC usage, an EU representative, data residency options and a Data Privacy Framework listing.
Read the GDPR guide and browse all vendors with evidenceQuestions buyers ask
Is Toku GDPR compliant?
There is no GDPR certification in general use. The verifiable facts are a public data processing agreement, standard contractual clauses, an EU representative and a Data Privacy Framework listing. See the legal artefacts and the DPF row on this page, each with its capture date.
How does CertReports verify this?
Every state carries a capture date, a source and a snapshot link. Registry rows come from the official registry data; vendor statements come from the vendor’s own page or trust centre; nothing is inferred. Vendors can dispute any row and corrections ship within two business days.
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