Evidence with its history
Source versions, review decisions and changes remain part of the record. Connected information keeps its provenance.
INTRODUCING UNESORA
From the first protocol to the final evidence. A modular platform designed to connect your data, your teams and your decisions.
A BDA Services platform · In development
Connected information.
Clear responsibility.
One platform vision.
Built around the whole study.
THE PLATFORM
A study should not lose its context every time it moves between teams. Unesora is designed to connect the clinical development lifecycle, while preserving where information comes from and who is responsible for it.
Choose the modules your study needs. Connect them to each other, or to existing systems through defined interfaces. Expand your scope as your needs grow.
Protocol, medical writing and study configuration.
Sites, participants, trial data and operations.
Safety, reconciliation and independent oversight.
Analysis, regulatory publishing and disclosure.
MODULAR BY DESIGN
Explore the full planned scope. Select a module to see its purpose and how it connects with the rest of the platform.
Product scope shown below is in development.Loading the module catalogue…
CONNECTED. WITH CONTROL.
Shared context does not mean unrestricted access. Our platform design puts provenance, responsibility and independence at the centre.
Source versions, review decisions and changes remain part of the record. Connected information keeps its provenance.
Study, site and role boundaries determine what each team can see and do. Treatment information requires distinct controls.
Adjudication and monitoring committee workspaces are designed around controlled data access, blinding and independent review.
A COMMON CONTEXT. DIFFERENT RESPONSIBILITIES.
Connect study planning, execution and evidence across the teams responsible for delivery.
Bring operational progress and clinical information into context, with discrepancies that can be investigated.
Carry source evidence into case review, aggregate reporting and regulatory work.
Purposeful workspaces with access defined for each role, study and responsibility.
A FEW USEFUL ANSWERS
No. The architecture is designed for separately configurable modules. A module can use another Unesora module or an approved external source for the information it needs, subject to the interface and study requirements.
No. Shared identifiers and defined connections provide continuity, while each module retains responsibility for its own records. Reconciliation preserves differences and source history rather than silently overwriting them.
Defined external interfaces and controlled imports are part of the platform design. Compatibility, transfer formats and validation need to be assessed for each integration.
Unesora is in development. This page presents its planned product scope and design principles. It does not claim that the modules are currently implemented, validated or available for live clinical use.
The design separates access to operational, clinical and treatment information. Adjudication and data monitoring committees have specific access boundaries; information is shared only within the applicable review scope.
START WITH WHAT YOU NEED
Choose the modules relevant to your study and download a short scope brief to use in your planning conversations.
YOUR PLATFORM SCOPE
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