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TrialSign provides scoped clinical intelligence advisory for biotech strategy and diligence.

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TrialSign provides research intelligence and strategic scientific analysis. It does not provide medical, legal, regulatory, patent or investment advice.

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Method

A transparent chain from question to conclusion.

TrialSign uses internal technology to support evidence collection, normalization, consistency checks and traceability. Analytical conclusions and strategic interpretation remain subject to human review.

01Decision question
02Evidence plan
03Source collection
04Normalization
05Critical appraisal
06Human review
07Deliverables

Workflow

Fourteen controls before a client deliverable.

01Decision framing

02Inclusion and exclusion criteria

03Evidence source plan

04Data cutoff

05Collection

06Normalization

07Deduplication and consistency checks

08Critical appraisal

09Claim-to-source mapping

10Confidence and uncertainty

11Human scientific review

12Client clarification

13Final quality gate

14Versioning and updates

Claim discipline

Different statements receive different labels.

The report does not treat facts, synthesis, interpretation and recommendations as interchangeable. This prevents unsupported conclusions from appearing as source facts.

01
Source record

Registry, paper, label or public company material

02
Structured synthesis

Normalized evidence object with source IDs

03
Interpretation

Analyst statement with confidence and limits

04
Client material

Decision Book, Dossier or private workspace view

Evidence typeUseConfidence note
Clinical registryPrimary status and design factsHigh when source-complete
Scientific literatureMechanism, outcomes and contextVaries by study design
Regulatory materialLabel and review contextHigh for approved claims
Patent researchPreliminary public IP contextRequires specialist review

Statement types

What the client can audit.

Verified fact

Directly supported by a primary or public source.

Structured synthesis

A normalized combination of source facts.

Interpretation

Analyst reading of what the evidence implies.

Hypothesis

A possible explanation that remains unconfirmed.

Evidence gap

A missing, weak or unresolved evidence element.

Recommendation

A proposed follow-up question or diligence action.

Next step

Bring the decision question, not a prepared search strategy.

Share the asset, target, indication or diligence question. TrialSign will identify the information needed to define a proportionate evidence plan.

Discuss a Diligence Question