Reduce clinical trial & research cost and time
Accelerate your drug trial & research timelines and reduce operational overhead by 67%. Aurora transforms fragmented patient-reported outcomes into standardized, EHR-ready AI insights for faster decision making.
The Challenge
Fragmented Data
Subjective symptoms often live in paper logs or siloed apps, making cross-comparison impossible
High Setup Friction
Building custom monitoring tools for every new cohort is slow, expensive, and technically taxing
Regulatory Hurdles
Converting patient diaries into audit-ready formats (FHIR/HL7) manually leads to human error
How we do it
AI Integrated Dashboard
Manage thousands of candidates and multiple trial groups from a single dashboard with all insights required to lean about all trial metrics
The DSR Engine
Automatically synthesize mood, medication, and symptom data into standardized CSV, JSON or PDF reports
EHR-Ready Data
Native support for FHIR/HL7 standards, ensuring seamless integration into existing hospital or research databases
Privacy-First Operation
Robust encryption with a user-led "Opt-In" model that simplifies your IRB and GDPR compliance
Beyond Clinical Trials: Vertical Expansion
Chronic Care Management (CCM)
Provide healthcare providers with a 'Digital Front Door.' Instead of waiting for the next appointment, doctors get real-time alerts if a patient's mood or symptom trends indicate a flare-up
Post-Market Surveillance
Pharmaceutical companies need to track real-world evidence (RWE) after a drug is cleared. Aurora automates the collection of long-term efficacy data and side-effect profiles at scale, without the cost of a full clinical trial
Precision Medicine & Research
Institutions studying the 'Correlation between Environment and Symptom' can use Aurora's intelligence layer to find patterns that human observation misses. We facilitate Faster discovery of therapeutic 'Aha!' moments through data-rich longitudinal tracking
Privacy-First Architecture
Shifting Agency to the Patient, Reducing Institutional Liability
The traditional data collection model forces institutions to take full "custody" of raw patient data, creating significant regulatory liability and ethical hurdles. Aurora flips the script. Aurora operates on a Permission-Based Synthesis model. Data remains private and encrypted within the Heylixir app until the user explicitly triggers a Data Sharing Report (DSR)
Patient Agency
Users maintain 100% ownership of their data. They choose what to share, when to share it, and who can see it
Reduced Institutional Liability
Because the transfer is user-initiated, your institution moves from being a 'Data Capturer' to a 'Data Recipient.' This significantly lowers the barrier for IRB (Institutional Review Board) approvals and Ethics Committee reviews
Ethical Alignment
Aurora aligns with the 'Right to Portability' under GDPR and the 'Patient Access' mandates of HIPAA, ensuring your trial or program is future-proofed against evolving privacy laws
More On Our Security
Explicit Opt-In (for patients)
Simplifies Informed Consent paperwork and 'Right to Withdraw' protocols
End-to-End Encryption
Data is encrypted at rest and in transit; Aurora never 'sees' unmasked data without authorization
Audit-Ready Logs
Every DSR generation is logged, providing a clear chain of custody for regulatory audits
Data Handling Flexibility
Institutions have the option to synthesize and export data to internal systems, then purge from Aurora to minimize data footprint
FAQ
Frequently Asked Questions
Have a question about Heylixir? Here are some answers to some of the most frequent questions you may have.