Protocols, approvals and consent forms kept in separate files
Trials registry
Every protocol with ethics approvals, team, consent forms and enrolment against target.
For researchers and research institutions
Research drawn from routine care, with governance built in.
A clinical research system and trials registry connected to the patient record. Find eligible patients, manage screening and consent, and export data without identifiers, with every query audited.
Studies need participants, data and governance that will satisfy an ethics committee and a sponsor.
For hospitals, research institutions, universities and ministries running studies.
Why it fits
What you get.
Clinical research and a trials registry built into the record. MOANA Clinical Research connects a trials registry and recruitment workflow directly to the clinical record, with privacy protections built in from the first query.
Finding participants means exposing who they are
Cohort discovery
Inclusion and exclusion criteria with live counts, before any identity is shown.
An audit trail rebuilt by hand for ethics review
Research governance
Role based access for investigators and coordinators, and a full audit trail for ethics review.
Research kept away from the point of care
Clinician trial alerts
Treating doctors see possible matches in the patient chart, and refer with one click.
Participant management
Screening, contact, consent and enrolment connected to each participant’s record.
International standards
Criteria and exports use ICD 10, SNOMED CT, LOINC and FHIR R4.
The applications behind it
Included modules.
How it works for you
Counts before identities, and every action audited.
Each step of a study is governed in the same system as the record it draws on.
- 1
Register the protocol
The trial is registered with its ethics approvals, team, consent forms and enrolment target.
- 2
Discover the cohort
Cohort discovery returns counts before identities.
- 3
Screen and consent
Treating doctors see possible matches in the chart, and consent is recorded against approved versions.
- 4
Export with approval
Exports remove identifiers and require approval, and every action is audited.
New
MOANA Clinical Research is now available.
Launched 20 October 2026A new system on the Moana platform for finding eligible study participants without exposing who they are.
Can sponsors see feasibility before a site is selected?
Yes. Network feasibility and sponsor reports provide eligible patient counts across facilities, without identities.
See Moana with your own workflows.
We will walk your team through the platform using the departments and reports you work with every day.