Research Labs
Structured data storage, consent management, and collaboration tools for multi-institutional genomic research. From population-scale GWAS to single-gene studies.
Safe • Secure • Yours.
A HIPAA-compliant genomic data platform for research, clinical care, and personalized medicine.
Genetic information is permanent and uniquely identifying. Unlike a password or credit card number, it cannot be changed. It reveals not only the individual from whom it was collected, but also their biological relatives — past, present, and future.
Current solutions are fragmented, poorly governed, and offer data subjects little meaningful control. Genomic data moves between research institutions, clinical laboratories, insurance companies, and commercial providers with inconsistent security standards and inadequate regulatory oversight.
In 2023, 23andMe suffered a data breach exposing the genetic profiles of 6.9 million users — a reminder that the consequences of inadequate genomic data governance are not hypothetical. The company filed for bankruptcy in 2025.
Actag exists to provide the infrastructure that the field has lacked: a purpose-built, HIPAA-compliant platform for secure storage, structured access, and patient-centric governance of genomic data.
Structured data storage, consent management, and collaboration tools for multi-institutional genomic research. From population-scale GWAS to single-gene studies.
HIPAA-compliant EHR integration for pharmacogenomics, cancer panels, and clinical decision-making. Designed for the workflows of health systems.
Secure personal genomic storage with physician access portals and concierge interpretation. Your genome, under your control.
Privacy-preserving architecture with zero-knowledge proofs and encryption at rest and in transit. Built for the most sensitive data class in existence.
Hybrid on-chain/off-chain design following the emerging technical consensus from 255 peer-reviewed papers spanning 2009–2026.
Patient-centric governance gives data subjects real control over who accesses their genetic information — not just a privacy policy, but enforced rights.