Keep ownership even when your CRO does not use Tenvia.
Build or import the protocol, review evidence, preserve decisions, bring in CRO recommendations and prepare execution requirements in an environment controlled by the Sponsor.
Tenvia Platform
Keep your systems. Run the study from one place.
Tenvia gives authorised teams one current view across protocol intent, relevant external evidence, the CRO operating plan, sites and existing clinical technology. Fewer vendor chases, fewer status decks and less manual reconciliation.
EDCCTMSeTMFIRTeCOALabsTrial recordsLiteratureRegulatory
The intelligent operating layerOne governed study.
Intent, relevant evidence, decisions and work remain connected.
No portal chasingEvidence in contextLess site burdenOne current truth
One operating model
Your technology stack was built to run systems.
Tenvia helps it run the study.
Start with one Sponsor or CRO team. Tenvia carries study intent into a structured execution blueprint, connected delivery and continuous oversight while preserving the option to bring partners into the same controlled context later.
Flexible adoption
Start with your team. Bring others in when the study needs them.
A Sponsor or CRO can use Tenvia independently. Shared access becomes useful when both teams need to work from the same study record.
Bring Tenvia to any Sponsor engagement.
Structure the study, challenge operational assumptions, prepare recommendations and create controlled outputs for the Sponsor as part of your delivery method.
When both teams connect, the handoffs disappear.
Sponsor intent, CRO expertise, external evidence and Tenvia analysis come together with explicit authority and one attributable decision history.
No rollout across the whole study is requiredBegin with the work that matters most, then expand.
- 01Start
- 02Extend
- 03Collaborate
- 04Connect
- 05Orchestrate
One continuous Tenvia system
Use evidence in design and keep it connected through execution.
Approved decisions, requirements, commitments and observations stay with the study through each handoff.
- 01Design the study
Protocol Intelligence
Use internally as a Sponsor or CRO, then share controlled outputs.
→ - 02Define execution
Study Blueprint
Send complete requirement packages externally. Vendors do not need an account.
→ - 03Source intelligently
Bid Room
Upload external proposals and compare them against one baseline.
→ - 04Connect execution
Study Connect
Connect authorised systems without forcing every organisation to change at once.
→ - 05Understand performance
Study Pulse
Monitor authorised execution even when partners continue to work externally.
Connect
Bring authorised information from the protocol, CRO plan, sites, specialist systems and relevant evidence sources into one study view.
Stop reconstructing the trial from vendor portals, searches and status decks.Understand
Use the study context to find relevant precedent and connect each insight to its source, assumptions, confidence and limitations.
Reach decisions faster without losing the evidence behind them.Control
Prepare the work, route the approval and record what was authorised, executed and verified.
Reduce coordination work while people retain clinical and commercial authority.One change, kept connected
From protocol decision to verified execution.
Follow one amendment without switching between documents, vendor systems and reconciliation spreadsheets.
- 01
Sponsor proposes
Amendment 3 changes eligibility. The approved baseline stays protected.
- 02
Tenvia finds relevant precedent
Comparable trials, reported outcomes, literature and regulatory material are matched to the study context where available.
- 03
The Study Blueprint updates
Population, sites, enrolment, burden and affected technology requirements remain traceable to the approved decision.
- 04
Vendors respond to one baseline
Technology and service proposals can be compared against the same scope, assumptions and dependencies.
- 05
CRO coordinates the work
A single owned work package replaces separate vendor and site chases while the Sponsor retains decision authority.
- 06
Systems execute and verify
Approved changes move through validated connector boundaries where supported, then return to the same study record.
Designed around authority
Observe. Assist. Act.
Capability increases only when evidence, validation and human authority support it.
Observe
Read or receive only the exact information authorised for this study.
Assist
Explain divergence and prepare attributable work for qualified review.
Act
Execute a supported operation only after authority, approval and verification are confirmed.
The availability and direction of each connection depend on the external system’s supported interfaces, customer permissions, validation requirements and the Tenvia connector’s release status.
Integration coverage
Connect the systems already running your trial.
Select a category to see what Tenvia can exchange, how the connection works and where approval remains with your team.
EDC
Study configuration, visit windows, eligibility flags, queries and tasks
- Data direction
- Read and write when supported
- Connection route
- APIs, events, structured files or controlled imports, according to the selected platform and authorised configuration.
- Approval
- Material configuration writes require authorised human approval
- System boundary
- The selected platform remains the system of record. The connection route is confirmed against its interfaces, customer permissions and validation requirements.
Connector availability depends on the selected platform, its supported interfaces and the customer’s authorised configuration. Tenvia confirms the connection route during technical scoping.
For the CRO
Use one operating model across every awarded study.
Set ownership, workflows and connection patterns once. Prepare controlled outputs for the Sponsor, then invite the Sponsor into the workspace when direct collaboration is appropriate.
The CRO can lead operations while the Sponsor retains clinical and contractual authority. Sites receive a simpler view of the work.The Sponsor does not need to adopt Tenvia first.
A single coordination model can cover every vendor.
Operating knowledge carries into the next study.
A controlled start
Begin with one study problem.
Start where disconnected work costs the most. Prove the value, then add the next system or study.
- 01
Operating map
Weeks 1 to 2. Map the current baseline, critical decisions, systems, owners and the reconciliation work that takes the most time.
- 02
Connection design
Weeks 2 to 3. Agree source objects, access, read and write boundaries, evidence and failure handling for the first systems.
- 03
Controlled pilot
Weeks 4 to 6. Configure the study model, test mappings and run the selected decision thread with fixture or approved data.
- 04
Validate
Led by the customer · Confirm permissions, data quality, audit behaviour, recovery and the qualified review route.
- 05
Activate & expand
After approval · Activate the agreed scope, monitor health and add the next system or study without rebuilding the operating model.
Bring the systems you already use