Gosta Research Program

Clinical AI built for
your evidence

The Gosta Research program gives investigators direct access to the models powering Gosta OS. Upload clinical notes, reports, or records, and Gosta turns them into structured, research-ready data.

How it works

The model layer for clinical research

The Gosta Research program is the first time we're making our clinical models available under a research license. Upload your clinical notes, reports, or records, and Gosta returns structured, research-ready data for your analysis. The models run in your environment of choice, supporting strict data locality and sovereign-AI requirements.

HOSTED

Gosta Document Intelligence

Run the models through our research web application. Ready to use, no infrastructure required.

LOCAL MODELS

Run models locally

Deploy Gosta models in your university's or health system's GPU infrastructure. The data never leaves your walls.

Models and capabilities

Specialized models with traceable outputs

Four purpose-built clinical models, validated across English, German, French, Swedish, and Finnish clinical text. More languages coming soon.

O1

Gosta OCR

Bring in the documents holding your structured data: clinical notes, reports and letters. OCR, layout parsing, and format handling.

PDF (scanned or native)
Common image formats
Plain text and clinical exports

O2

Gosta PII detection and removal

Dedicated models that find personal identifiers in your clinical text and remove or mask them so the data can be processed safely.

Names, dates, IDs, locations, and contact details
Mask or fully redact, configurable per study
Validated for multiple languages

03

Gosta Clinical coding

Map free-text clinical content to standard clinical coding terminologies.

International standards such as ICD-10 & ICD-O morphology
Confidence scores
Built for clinical text across specialties

04

Gosta Clinical data extraction

Detect and extract defined clinical variables from unstructured documents.

Adverse events (CTCAE), performance status (ECOG), staging (TNM)
Biomarkers and medications
Span-grounded: every value points to the source text
Getting access

Four steps from application to access

01
Apply

Submit your study details. We verify your registry record and IRB status.

02
Review

Our research access committee evaluates eligibility. Decision in 5-10 business days.

03
Onboard

We sign the DPA and research licence, then issue credentials in your region.

04
Run

Use the models in your research. Export model performance metrics on your cohort for publication.

Eligibility

Free for academic and non-commercial research

WE'RE A FIT
Investigators at universities, hospitals, and research institutes
Studies with IRB/ethics approval, under review, or documented exemption
Registered protocols on ClinicalTrials.gov, CTIS, ISRCTN, or an institutional registry
Industry-funded studies where the investigator retains publication rights
NOT IN SCOPE HERE
✗ Commercial product development
✗ Research without ethics oversight
✗ Redistribution of model outputs as a derived product

✗ Clinical use in routine patient care: reach out to us to learn about routine care access.
Apply for access

Tell us about your study

We review every application against our research-access policy. Most decisions within 5-10 business days.

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