Tenvia Clinical Agents

Clinical development, operated through intelligent agents.

Tenvia assembles specialist clinical intelligence around the objective you are trying to achieve while preserving evidence, permissions and human authority.

TENVIA-204Objective plannerIllustrative product model

Tenvia assembles

Design my study.

01Protocol Intelligence

02Evidence

03Feasibility

04Regulatory

One Study Agent

The study is the organising principle.

The Study Agent works from the governed study state rather than a loose conversation history. Objectives, protocol, evidence, assumptions, decisions, vendors, systems, performance and amendments remain connected through the Study Graph.

Not separate AI personalities. Specialist capabilities inside one governed operating model.

Study objectiveStudy GraphStudy AgentClinical agentsHuman decision

Specialist clinical intelligence

Assemble the work the objective requires.

Each capability receives only the study context, tools and permissions required for its task.

Protocol Intelligence

Understands the proposed design and surfaces its scientific and operational consequences.

Evidence

Retrieves relevant precedent and keeps sources, match logic and limitations attached.

Regulatory

Surfaces relevant guidance and public regulatory context for qualified review.

Feasibility

Tests recruitment, countries, sites and delivery assumptions against the study.

Technology

Derives system requirements created by the approved study design.

Procurement

Structures vendor requirements and normalises responses for comparison.

Study Oversight

Explains what changed, why it matters and what the team may consider next.

Tenvia is being built around an extensible clinical agent architecture. Individual capabilities will become available by release stage and authorised use.

Governed autonomy

Intelligence that knows when to act and when to ask.

Observe

Retrieve, compare, inspect and calculate within authorised boundaries.

Propose

Prepare recommendations and alternatives without changing governed study state.

Commit

Act on an approved study or external system only after human authorization.

Approval required

From general intelligence to governed clinical intelligence

Generic AI gives your team intelligence. Tenvia gives that intelligence a governed understanding of the study.

Tenvia does not expand your access.

If a user cannot access a study, document or connected system record, the agent is designed not to make it accessible simply because AI is involved.

Explore Security & Trust

Bring a real objective

What would you ask Tenvia to accomplish?

Start with a study concept, protocol or active trial. We will map the specialist intelligence, evidence, systems and approval boundaries required.

Illustrative interfaces describe the intended product architecture and workflow. They do not imply every agent or external action is currently production-ready.