The platform

Three pillars outside. Four stages inside.

Trovensa is being designed as one platform for a drug-development program: evidence in context, work with continuity and decisions with a record, across discovery, preclinical development, clinical development and manufacturing planning.

Programs as the working scopePermission-gated actionsAudit of every changeAgent action recordsApproval recordsVersion history

Three pillars outside

Three pillars outside, four stages inside.

The pillars are how the platform is described. The stages are the lifecycle the records move through. Every product belongs to one pillar and would work from the same records, permissions and evidence.

Pillars, products and status
PillarWhat it meansProductsStatus
CONTEXTEvidence in context
Keep sources, findings, interpretations and open questions connected.
Designed
CONTINUITYWork with continuity
Carry context between approved tools, plans, records and reviews.
Designed
RECORDDecisions with a record
Preserve reviewer decisions and the history of agent actions.
Designed

01 / Discovery

Turn a question into evidence-supported next steps.

Trovensa is being designed to help researchers investigate questions, identify knowledge gaps and develop evidence-supported research plans.

Intended outcomeA research question with its sources, findings, gaps and proposed hypotheses connected and labelled.

Compare findings

Agents would examine authorised literature, internal documents, historical experiments and datasets to compare findings and surface contradictions.

Propose hypotheses

Each proposed hypothesis links back to its supporting and contradicting evidence for scientific review.

RecordsResearch questionsSourcesFindingsHypothesesKnowledge gaps

02 / Preclinical development

Keep the plan, the protocol, the data and the interpretation connected.

During research execution Trovensa would connect with the tools scientists already use rather than replace them: protocols, electronic lab notebooks, approved analytical and design tools, and report drafting.

Intended outcomeA plan whose protocol, experiments, results and interpretation remain linked as work repeats and branches.

Prepare a draft

Agents would prepare protocol and report drafts for a scientist to review, edit and approve.

Carry context

Context would move between activities so a question, its plan, the resulting data and the interpretation stay connected.

RecordsResearch plansProtocolsExperiment recordsDraft reports

03 / Clinical development

Review records against approved procedures, with the source in view.

Trovensa would compare research records with approved standard operating procedures and document requirements, presenting each finding with its source, the requirement and an explanation for review.

Intended outcomeReview findings a quality reviewer can accept, dismiss or resolve, each traceable to a record and a requirement.

Surface potential gaps

Missing metadata, unsupported conclusions, inconsistent entries and potentially undocumented deviations would be surfaced for review, never treated as proof.

Record the decision

Reviewer decisions, versions and agent actions would be kept as a record without silently changing approved scientific records.

RecordsStandard operating proceduresReview checksReview findingsDeviations

04 / Manufacturing planning

See the program as one connected picture.

Across discovery, preclinical and clinical development and manufacturing planning, Trovensa would maintain a connected view of program progress.

Intended outcomeMilestones, dependencies, responsibilities, supporting evidence, outstanding questions and approvals in one place.

Track progress

Teams could track milestones and dependencies while accommodating parallel activities and repeated experiments.

Reduce lost context

The long-term ambition is fewer manual handoffs and less lost context between stages and teams.

RecordsMilestonesDependenciesOpen itemsApproval records

Agents propose, people decide

Agents prepare, compare, propose and flag. An authorised person decides.

Nothing an agent produces would become a scientific record on its own. Every proposed item is intended to wait for a named person with the permission to decide.

  1. 01

    Agents prepare

    Agents would compare sources, prepare drafts and check records against approved procedures, inside the permissions of the program.

  2. 02

    Every statement is labelled

    Each finding, hypothesis and proposed step carries an assertion kind and an origin, so a reader can tell an observation from a suggestion and a person from an agent.

  3. 03

    A person decides

    An authorised scientist, reviewer or program lead accepts, rejects, dismisses or resolves each item. Approval records carry the decision and its rationale.

  4. 04

    The record stays

    Agent action records, version history and audit entries are intended to remain readable after the work moves on.

The connected program view

See the program as one connected picture.

Progress is being designed to show milestones, dependencies, open items and approvals by stage, each linked to the evidence behind it. The lanes below are an illustrative sketch of that view.

Illustrative program TRV-101Illustrative

01 Discovery

  • Question: candidate pathway
  • Finding comparison (agent-generated, labelled)
  • Hypothesis: accepted

02 Preclinical development

  • Plan A
  • Protocol v2 (draft)
  • Experiment 14 and repeat

03 Clinical development

  • SOP check: sample handling
  • Finding: open
  • Deviation: none recorded

04 Manufacturing planning

  • Milestone: planning question
  • Dependency: blocked
  • Open item: owner needed

Illustrative example; the view is designed and has not been built.

Illustrative flows

Flows that end in a decision.

Each flow is an illustrative example of how the products would connect. Agent steps are labelled; the last step is always a person deciding.

01 · Discovery

Investigate a question

  1. Register the question
  2. Attach authorised sources
  3. Compare findings (agent-generated, labelled)
  4. Accept or reject hypotheses

Trovensa Evidence

Illustrative flow
02 · Preclinical

Run the plan

  1. Write the plan
  2. Prepare a protocol draft
  3. Record experiments and repeats
  4. Approve the report

Trovensa PlansTrovensa Progress

Illustrative flow
03 · Clinical

Review against an SOP

  1. Choose the SOP and the record
  2. Run the check
  3. Decide each finding
  4. Track deviations to closure

Trovensa Review

Illustrative flow

Connections

The tools scientists already use stay where they are.

Trovensa would connect with the systems a program already runs on rather than replace them. Nothing is connected today; every connection is a design target.

Available today

None available today.

Next

None.

Designed forDesigned
  • Electronic lab notebooks over REST
  • Literature search services
  • Document libraries
  • Approved analytical and design tools
  • Enterprise identity providers such as Microsoft Entra ID

Read on

The documentation carries the reference pages and the decision log.