Tenvia Study Blueprint

From protocol to executable study.

Once the design is approved, Tenvia translates the study into the technology, data and operational requirements needed for execution. Vendors can collaborate in Tenvia or receive the package externally.

Follow the study ↓
Approved study inTraceable requirements outOne pricing baselineHuman authority retained

Continuity after approval

The protocol defines the study.
Tenvia turns it into an execution blueprint.

The approved study should not disappear into disconnected RFPs, spreadsheets and vendor conversations. Its decisions should remain connected through sourcing, configuration and live delivery.

One continuous Tenvia system

The study remains the centre.

  1. 01Design the study

    Protocol Intelligence

    Understand evidence, feasibility, risk and consequence.

  2. 02Define execution

    Study Blueprint

    Translate the approved study into technology, data and operational requirements.

  3. 03Source intelligently

    Bid Room

    Compare technology and service proposals against one common baseline.

  4. 04Connect execution

    Study Connect

    Carry approved requirements into the systems and vendors responsible for delivery.

  5. 05Understand performance

    Study Pulse

    Know when actual execution begins to diverge from the plan or commitment.

Sponsor and CRO study professionals reviewing a shared execution specification
The approved study and its shared specification

Owned by the Sponsor. Ready for collaboration.

Give every delivery partner the same study without requiring the same tool.

The Sponsor retains decision authority. CROs and specialist providers can contribute inside Tenvia or through controlled external inputs and outputs, without recreating what the study requires each time.

Capability before vendor

Determine what the study requires first.

Tenvia begins with the required execution capability and the reason for it. Vendor selection comes later.

Approved study signals
  • Randomised
  • Blinded
  • Multiple treatment arms
  • Investigational product supply across 12 countries
Protocol and supply decisions remain linked
IRT / RTSMRequired
01

Required to support randomisation, blinding and investigational product supply across countries and sites.

RandomisationStratificationKit assignmentDepot managementSite inventoryResupplyEmergency unblindingEDC integration
Reason and source decision inspectable

Requirements ready for vendors

Give every vendor the same clear scope.

Generate one professional requirement baseline that vendors can price externally. No vendor account is required.

Study Technology Blueprint
Illustrative structured output · v1.0
01Study overview02Countries03Sites04Subjects05Arms06Visits07Study duration08Enrolment assumptions09EDC complexity10Forms and domains11Integrations12Randomisation13Drug supply14eCOA instruments15Languages16Lab requirements17Safety requirements18Validation expectations19Reporting20Implementation assumptions21Vendor dependencies
What is requiredWhy it is requiredTraceable to the approved study

Comparable proposals

Compare the requirement,
not just the number.

Upload proposals received outside Tenvia and normalise them against one Study Blueprint. Vendors do not need to change how they respond on day one.

Tenvia comparison · Proposal BThe lowest headline quote may become the highest once missing scope is normalised.
50 sites pricedLab integration excludedData migration excluded
Illustrative pricing and normalisation only. Final scope and price remain subject to vendor confirmation and authorised commercial review.

Commercial neutrality

The study first.
The vendor second.

Tenvia starts with what the study requires, not which vendor is selling it. Recommendations should remain explainable against objective study and delivery factors.

01Study fit02Required functionality03Integration compatibility04Geographic coverage05Timing06Commercial assumptions07Price

Future direction for structured pricing

Use governed pricing logic to clarify budgets earlier.

Where participating vendors provide approved pricing structures, Tenvia can apply them to the Study Blueprint without implying that every vendor supports instant pricing.

Base fee+Per site+Per subject+Countries+IntegrationsIndicative price approved by the vendor
For Sponsors

Turn an approved study into a clear technology strategy.

Use Tenvia internally and give existing CROs and vendors controlled requirements without requiring their adoption.

For CROs

Translate design into delivery for any Sponsor.

Prepare a controlled execution specification and a clear output for the Sponsor without requiring the Sponsor to use Tenvia.

Clinical research colleagues reviewing study execution requirements in a modern trial setting

Blueprint to Study Connect and Study Pulse

Do not let the requirement become a disposable RFP.

The same structured requirement should continue through selection, configuration and execution so teams can compare what the study required with what was committed, configured and observed.

  1. 01Required
  2. 02Committed
  3. 03Configured
  4. 04Actual
See the connected platform

Bring one approved or developing study

See what it will take to execute.

Start with Protocol Intelligence