How we work before we are contracted for a specific protocol

1

Our in-house physicians build data dictionaries specializing our algorithms to disease types

2

We work synergetically with trial site IRB’s to keep all data queries within their healthcare systems firewalls in a regulatory compliant manner. Only trial site research teams are able to identify their own patients.

3

Our NLP extracts clinical datapoints relevant for clinical research protocols

How pharma sponsors can contract with us

1

Mutual CDA’s signed

2

We scope your protocol for patient population size, complexity of criteria and data point availability

3

We provide you with a proposed plan of action to match de-identified patients to trials, along with timeline and cost

Once we are working with pharma sponsors on a live contract

1

We work with healthcare systems within our partner network and/or pharma’s trial site network for approvals, compliance, and observational clinical study data

2

Our studies take the purpose of one of the following use cases for specific disease indications:

Synapsis

Analyze Biomarkers over time

Research

Create synthetic control arms

Patient Predict

Enrollment Allocations

Patient Finder

Pre-qualify patients on more than 80% of your most complex protocol criteria