Vivabioma™ Privacy Policy
Version VB-PP-2026-01 · Effective September 14, 2026 · Replaces version of March 1, 2026 ·
1. Who is responsible
- General contact: info@vivabioma.com · Phone: +34 960 090 596
- Privacy and exercise of rights: lopd@tellmegen.com
- Data Protection Officer: dpo@tellmegen.com
- Supervisory authority: Spanish Data Protection Agency (www.aepd.es) or the supervisory authority of your country of residence.
2. Who this Policy applies to
3. What data do we process and where does it come from
- Account and contact: name and surnames, email, encrypted password, date of birth, sex if provided, address, phone, language, and country.
- Biological sample: feces collected with our kit.
- Analysis data: sequencing and quality control technical data, microbiome profile, estimated functions, indices and resulting reports.
- Questionnaire responses on diet, habits, symptoms, and well-being. Optional questions are identified as such; omitting them may limit the content that depends on them.
- Hiring and payments: orders, invoicing, extensions and transaction metadata. We do not store full card numbers.
- Platform Usage: accesses, reports consulted, downloads, functions used, metrics and data collected via cookies.
- Customer service communications and incident records.
- Documentation proving legal representation or support measures, when contracting for a minor or a person requiring support.
4. Nature of incidental human data and DNA
5. What we use your data for and on what legal basis
- Register the sample, sequence, filter, generate, host, and update your reports: contract execution (Art. 6.1.b) and explicit consent for health-related data and other special categories, including incidental human fragments (Art. 9.2.a).
- Create and manage your account, logistics, access to reports, and extensions: contract execution (Art. 6.1.b).
- To attend to their rights and requests for access and portability: legal obligation (Art. 6.1.c).
- Verify identity, legal representation, and support measures, and prevent unauthorized analysis: compliance with applicable legal obligations (Art. 6.1.c) and, where no specific obligation exists, legitimate interest in preventing illicit or fraudulent uses (Art. 6.1.f). The preservation of proof of consent and representation is also covered by Art. 9.2.f.
- Improve the service and guarantee its security, prevent fraud and defend claims, through aggregated or anonymized analysis whenever possible: legitimate interest (Art. 6.1.f), with the right to object.
- Fulfill legal obligations regarding taxes, commerce, health, quality, and product surveillance, and respond to authorities' requests: legal obligation (art. 6.1.c).
- Research and development, including the training of artificial intelligence models, in the areas described in paragraph 20 of the Informed Consent: your specific and separable consent (Articles 6.1.a and 9.2.a). The combination of data with another GENELINK service requires separate and additional consent.
- Professional Access: your specific consent provided by activating it.
- Transactional and support communications: contract execution (Art. 6.1.b).
- Electronic commercial communications: your consent or, for products and services similar to those already contracted, the legitimate interest provided for in the regulations on information society services, with the possibility of unsubscribing with each shipment.
6. Research, development and artificial intelligence
7. Minors and persons with support measures
8. Automated decisions
9. The biological sample
10. Conservation, extensions, and blocked archive
- Account and contract: during the relationship and, afterwards, during the applicable statutes of limitations.
- Invoicing and accounting: within the deadlines required by commercial and tax regulations.
- Biological sample: in accordance with section 9.
- Microbiome Profile, Technical Data and Reports: as long as your account is active, so you can consult them, compare them and request extensions.
- Technical and safety records: between 12 and 24 months, proportionally to their purpose.
- Supporting documentation for representation and registration of consent acceptance: as long as liability can be incurred.
- Research: according to the project duration or until the authorization is withdrawn, with the exceptions of section 6.6.
11. Recipients, supervisors, and deputy supervisors
- Metagenomic sequencing laboratories, which receive the coded sample.
- Infrastructure, hosting, storage, and security providers.
- Gateways and payment providers.
- Logistics operators.
- Support, communication, and analytics tools.
- Research collaborators, when you have authorized it and with pseudonymized or anonymized data.
- Authorities and public bodies, when there is a legal obligation.
