Quality • Regulatory • Privacy
Standards you can verify
Laboratory quality, regulatory status, data protection and ethics are published as documented facts. Where documentation is not yet available, we say so.
Credentials
No generic badges
Each credential will link to its certificate, issuing authority, certificate number, scope and expiry date. Relevant frameworks, such as laboratory licensing, ISO, CAP, CLIA, CE IVD or IVDR and local Ministry of Health authorisation, are listed only where they apply and are confirmed.
Laboratory
- LicenseDocumentation to be provided
- AccreditationDocumentation to be provided
- Quality systemDocumentation to be provided
Test
- AuthorizationDocumentation to be provided
- Intended useDocumentation to be provided
- ValidationDocumentation to be provided
Data
- PrivacyDocumentation to be provided
- ConsentDocumentation to be provided
- RetentionDocumentation to be provided
- SecurityDocumentation to be provided
Ethics
- Medical oversightDocumentation to be provided
- Conflict disclosureDocumentation to be provided
- Responsible communicationDocumentation to be provided
Laboratory standards
How quality is controlled
- 01
Sample handling standards
Documented collection, stability, transport and rejection criteria for each validated specimen type.
- 02
Quality control
Predefined acceptance criteria at each analytical stage; failing samples are not reported.
- 03
Analytical validation
Accuracy, precision, reproducibility and limits characterised for the final assay.
- 04
Clinical validation
Performance in relevant clinical populations for a defined intended use.
- 05
Reference population
Documented characteristics of the reference data used by reported models.
- 06
Change control
Versioned methods and models, with the version recorded on every report.
Privacy, data & ethics
Epigenomic information requires a higher standard
Epigenomic data is personal medical information. It calls for more careful handling, and clearer communication, than an ordinary wellness questionnaire. Full policies will be published once finalised.
- 01
Consent
Informed consent describing what is measured, stored and for how long.
- 02
Data handling
Defined processing, access control and internal responsibility.
- 03
Storage & retention
Documented storage locations, encryption and retention schedule.
- 04
Confidentiality
Results are medical information and are treated as such.
- 05
Secondary use
No research use of identifiable data without explicit, separate consent.
- 06
Withdrawal
A defined process for withdrawing consent and requesting deletion.
- 07
Responsible interpretation
Communication designed to avoid over-interpretation or alarm.
- 08
Ethics oversight
Independent review of claims, content and communication.
Governance FAQ
Common questions
Generic badges communicate nothing verifiable. When a credential exists, it will be published with its certificate, issuing authority, number, scope and expiry date.
No authorisation is claimed. Regulatory documentation to be provided; the platform states status explicitly rather than implying approval.
Access is limited to the personnel required to deliver and interpret the result, under the approved data-protection framework.
Not without explicit, separate and revocable consent.