Enterprise Agentic AI for Pharma | Accelerate R&D with AI Agents

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Stop Risking Compliance. Start Accelerating Discovery.

Agentic AI for Pharma

Governed, Explainable, and Audit-Ready.

Give your R&D scientists, regulatory affairs teams, and clinical operations instant answers from study reports, CTDs, trial data, and internal research with full source traceability, explainability, and zero hallucination risk.

Accelerate evidence discovery — find answers across studies, submissions, and trials in seconds, not hours
Eliminate compliance risk — every AI answer is traceable, explainable, and ready for FDA/EMA audit inspection
Reuse institutional research — surface prior studies, protocols, and regulatory decisions your teams have already produced
Governed AI by design — enforced access rights, full audit trails, and no data leaving your validated environment
Trusted by Pfizer, AstraZeneca, Takeda, and leading global pharma organizations

See how Enterprise Agentic AI works with your data, your security model, and your use cases.

Why Generic AI Fails in Regulated Pharma

Your R&D teams are re-reading studies that already answered the question. Your regulatory affairs teams are manually searching across submission dossiers that could be queried in seconds. Your clinical teams are waiting days for evidence that lives somewhere in your document management system.

Generic AI tools make this worse, not better. They hallucinate. They can’t cite sources. They fail audit inspections. And they put compliance at risk the moment an ungrounded answer reaches a regulatory submission.

Sinequa is built differently. Every answer is grounded in your validated pharma data. Every response is traceable. Every access event is logged. AI built for regulated pharmaceutical environments — not experiments.

Agentic AI Grounded in Your Data, Not Guesswork

Sinequa is built on Retrieval-Augmented Generation (RAG) — the architecture that makes AI safe for regulated environments. Every answer is retrieved from your internal validated data, not generated from a generic model trained on the internet.

What this means for pharma teams:

Every answer cites its source — document name, version, section — so your team can verify before acting
No hallucination risk — responses are constrained to your validated, internal content
Full audit trail — every query, every answer, every source is logged for regulatory inspection
Access-controlled — users only see answers from data they are authorized to access under your security model

What Sets Sinequa Apart

Built for regulated pharma

not adapted from a generic enterprise tool

Grounded in your data

CTDs, CSRs, IND submissions, trial reports, SOPs, and lab notebooks

Explainable by design

every answer cites its source so your teams can trust and verify

Trusted by the World's Leading Pharma Organizations

faster biostatistician data inquiries

faster time-to-market for therapies

$0M

saved with Phase 1/2 pass/fail ratio improvements

Agentic AI Built for Every Pharma Function

AI Agents for R&D & Research

Give scientists instant access to prior studies, protocols, and experimental results across your entire research repository.

AI Agents for Regulatory Affairs

Surface evidence across submissions, dossiers, and trial documentation — with the traceability regulators require.

AI Agents for Clinical Operations

Connect clinical teams to trial data, protocols, and safety reports without switching between systems.

Governance & Compliance by Design

Enterprise governance built in — not bolted on.

With Sinequa, we are building powerful next-generation search that is simple and intuitive enough for our R&D scientists to use easily and be alerted
to new information anywhere, anytime.

Nick Brown, Technology Incubation Director, Astrazeneca

Sinequa is simply great technology. We immediately saw its benefit watching it perform something we didn’t know was possible. It makes an exponential difference for our organization. We were also impressed with the number of smart connectors available out-of-the-box and Sinequa’s unique ability to develop new ones.

Oliver Thoennessen, Senior Manager Global IT Drug Development, UCB

If Siemens only knew what Siemens knows; that was the initial challenge... now our employees find insight more efficiently - we're 30% faster with Sinequa.

Dr. Thomas Lackner, CTO Office, Corporate Technology, Siemens

See How Sinequa Works With Your Data

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