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For biotech

Give AI the full scientific and business context behind every program.

Percidian connects programs, assets, targets, indications, studies, sites, endpoints, evidence, safety signals, submissions, milestones, partners, decisions, and dependencies into one governed, permissioned understanding — so every approved AI system sees what changed, what it affects, who owns the next decision, and which evidence supports it. A finding on a shared mechanism, vendor, site, or supplier lands on every program that depends on it.

Program and partner boundaries applied before context reaches AI · Every point cited to its source

Shared across programs

One safety signal. Every program it touches.

A single-asset company reads a safety review as one program’s problem. A portfolio cannot afford to. One shared dependency, every program it reaches.

Safety signal · ALT elevation · class effect. Seen first in BX-214’s Phase 2 review. BX-301 and BX-118 share the mechanism, so the safety review reaches three programs — not one. Reaches 3 of 4 programs.

Four programs — BX-214 (Phase 2), BX-301 (Phase 1), BX-118 (Phase 3), BX-407 (Preclinical) — and four shared dependencies: Safety signal, ALT elevation · class effect, touching BX-214 and BX-301 and BX-118; Vendor, Meridian Clinical · CRO, touching BX-214 and BX-118; Site, Site 14 · enrolling, touching BX-301 and BX-118; Supplier, Drug substance · single source, touching BX-214 and BX-407. Now lit: Safety signal · ALT elevation · class effect. Seen first in BX-214’s Phase 2 review. BX-301 and BX-118 share the mechanism, so the safety review reaches three programs — not one.

Illustrative example

The brief

Move from new evidence to the next decision.

One program memory across AI

Keep the program intact across every approved AI experience.

Research agents, clinical workflows, regulatory assistants, diligence tools, and executive AI draw from the same governed program understanding. Teams do not reintroduce the asset, rebuild its history, or reconcile competing versions of the evidence every time they change applications.

Approved source material becomes persistent program understanding that works across AI applications without repeatedly loading complete histories — inside each team’s permissions, with every point linked to its source.

Outcomes
  • Persistent program memory
  • Cross-functional context
  • Role-specific permissions
  • Source-linked evidence

The biotech ontology

Built on the available Biotech ontology, extended by your science and operating model.

Your naming, development stages, evidence standards, and governance extend it.

Legal pack — Matter, Party, Claim, Filing, Obligation, Deadline, Precedent · 9 types · depends on coreLegalLegal tech pack — Document system, workflow, e-discovery, billing entities · 6 types · depends on core, legal, techLegal techM&A pack — Target, Deal, Workstream, Diligence finding, Exposure, Condition · 9 types · depends on core, legal, fin, bizM&AFinance pack — Instrument, Holding, Exposure, Valuation, Covenant, Forecast · 16 types · depends on core, legalFinanceFintech pack — Account, Payment, Ledger, Rail, Provider · 6 types · depends on core, legal, finFintechBusiness pack — Company, Unit, Product, Customer, Contract · 5 types · depends on coreBusinessSales pack — Account, Opportunity, Quote, Renewal, Owner · 7 types · depends on core, biz, finSalesPeople & HR pack — Role, Employment, Compensation, Policy · 6 types · depends on core, finPeople & HRLife sciences pack — Program, Compound, Study, Site, Endpoint, Safety signal, Submission · 8 types · depends on core, legalLife sciencesTechnology pack — System, Service, Incident, Release, Dependency · 7 types · depends on core, legalTechnologyACEFoundation

The available Biotech ontology models programs, assets, compounds, targets, mechanisms, indications, studies, protocols, cohorts, sites, investigators, endpoints, results, evidence, safety signals, submissions, regulators, milestones, vendors, partners, intellectual property, obligations, decisions, owners, and source records. The organization’s own naming, development stages, evidence standards, governance, portfolio model, and decision process extend that shared structure without creating another silo.

Give biotech AI the program, not just the documents.

Bring scientific evidence, development history, regulatory context, decisions, and dependencies into one permissioned understanding that works across AI.

Bring your business into every AI decision

Give every approved AI system the context to do its best work.

Connect the knowledge your organization already has. Preserve what it learns. Apply the permissions it already trusts. Make that understanding available wherever people and agents work.

See it on your business.

A briefing mapped to your systems, your permissions, and one workflow that matters.

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