A network of 80+ partner hospitals and 1,500+ doctors across India, for licensed archives, new collections to your protocol, and annotation by practising specialists.
Multisite, specialist annotated datasets in neurology and pathology, including a 700 EEG dataset built from scratch. The same model works for any specialty.
Neurology · EEGClient name withheld
700 hour long EEGs, built from scratch
The data an EEG analysis company needed did not exist anywhere. We designed the collection with neurologists and recorded deidentified, hour long EEGs across multiple partner hospitals. Positive recordings carry an average of 86 annotated events each, marked by multiple neurologists with a defined protocol for resolving disagreements. Ethics committee approval and commercial use rights were signed for every recording.
150 epilepsy
550 without epilepsy
86 events per positive EEG
EDF format
700Annotated hour long EEGs
Pathology · HistopathologyClient name withheld
Multisite annotated histopathology
A medtech company needed histopathology data for product development. We sourced cases from pathology partners across several sites, annotated by pathologists.
MultisiteAnnotated by pathologists
How it works
From hospital records to datasets you can use.
Scope and feasibility
Tell us the data, volume, criteria and use. Within one to two weeks you get sources, timeline and price.
Free feasibility review
Sample data where available
Approvals and collection
We secure ethics clearance and data agreements, then license or collect across partner sites.
Ethics committee approval
FDA, HIPAA and UK GDPR aligned
Annotation and delivery
Specialists label to your guidelines. You receive secure transfers with a data card and QA report.
Cleared by each hospital's ethics committee, following ICMR guidelines.
Deidentified at source
Identifiers removed inside the hospital to HIPAA standards. Reidentification is contractually banned.
FDA ready documentation
Documented protocols, audit trails and quality records to support FDA submissions.
UK GDPR and DPDP
Agreements aligned with UK GDPR, the Data Protection Act 2018 and India's DPDP Act.
Full provenance
Source, dates, devices and consent recorded for every dataset.
Quality checked annotation
Multiple readers, adjudication and agreement metrics on every batch.
Who we work with
For any team that needs real clinical data.
Medtech and devicesDiagnosticsPharma and CROsAI and softwareAcademic research
FAQ
Common questions.
What is the difference between licensing and custom collection?
Licensing uses data hospitals already hold, so it is faster. Custom collection creates new data to your protocol. Many programs combine both.
Do you only work in neurology and pathology?
No. Those are our delivered programs so far. Our partner hospitals cover most specialties, including cardiology, radiology, ophthalmology and dermatology.
Can the data meet FDA, HIPAA and UK requirements?
Yes. We build datasets to FDA standards, deidentify to HIPAA standards, and handle processing and transfer in line with UK GDPR and the Data Protection Act 2018.
Can you annotate data we already have?
Yes. Share your data under a data agreement and our specialists will label it to your guidelines.
How quickly can we get data?
Feasibility in one to two weeks. Licensed data usually ships within weeks of approval. Custom timelines are agreed up front.
Can we evaluate a sample first?
Yes. For most licensed data we can share a small sample before you commit.
Is the data exclusive?
Licences are shared by default. Exclusive terms are available, and custom data can be yours alone.
Do you work with smaller teams?
Yes. We work with startups, research groups and large companies, and can scope small pilot datasets.
Contact
Tell us what you need.
Send a short brief. We reply with sources, timeline and price.