Cohere for Pharma & Life Sciences
Sovereign AI agents for pharma, life sciences, and regulated healthcare workflows.
Cohere helps pharma and life-sciences companies connect fragmented information from research, clinical development, regulatory affairs, medical affairs, quality, manufacturing, supply chain, and commercial operations with controllable AI workflows. North, Cohere’s agentic AI platform, brings secure reasoning into the systems, documents, and decision processes that run regulated pharma organizations — with sovereign deployment options, role-based access, audit-grade traceability, and governance for sensitive research, patient, product, and operations data.
For R&D, Clinical and Medical Teams
Find scientific evidence faster, structure study information, and prepare medical content consistently.
For Regulatory, Quality and Safety Teams
Analyze and document dossiers, deviations, CAPAs, SOPs, audits, safety signals, and regulatory requirements faster.
For IT, Data, Security and Compliance
Introduce AI under controlled conditions — with sovereign deployment, access controls, logging, and governance for regulated environments.
Powered by North
Find evidence. Understand risk. Act with control.
North turns complex pharma data and document landscapes into governed AI workflows for companies that need speed — without losing control over data, quality, compliance, or decision processes.
Understand faster
Search, summarize, and compare literature, clinical documents, regulatory dossiers, SOPs, quality data, safety information, and internal knowledge faster.
Connect the dots
Connect R&D, Clinical, Regulatory, Quality, Manufacturing, Pharmacovigilance, Medical Affairs, and commercial data into contextualized workflows.
Keep humans in control
AI agents prepare analyses, drafts, and recommendations — with sources, role permissions, approvals, audit trails, and documented decisions.
Pharma is ready for AI that works in regulated workflows.
The greatest value comes when AI does more than generate text — when it works across scientific evidence, regulatory documents, quality processes, and operational systems — sovereign, traceable, and integrable into existing GxP and compliance structures.
Regulatory & Submission Productivity
Help teams search, summarize, and prepare regulatory content, including dossier navigation, response drafts, change comparisons, and authority communication.
Quality & Manufacturing Intelligence
Analyze deviations, CAPAs, change controls, batch records, SOPs, audit findings, and production signals faster — with documented sources and controlled approvals.
Medical & Scientific Knowledge Workflows
Accelerate literature research, medical information, MSL prep, scientific Q&A, congress analysis, and internal medical knowledge search.
Pharma agents that build trust step by step.
Start with read-only analysis and knowledge search. Then expand into review support, draft generation, approval workflows, and controlled automation as teams gain confidence.
Search and compare dossiers, modules, variations, HA questions, labeling documents, and authority correspondence. Create summaries, response drafts, and impact analyses with source citations.
Support deviation analyses, CAPA reviews, change controls, audit prep, SOP search, and quality risk assessments — with role permissions, approvals, and documented traceability.
Analyze case reports, literature signals, safety narratives, product complaints, and signal information. Support triage, case summaries, and consistent documentation.
Compare study protocols, amendments, investigator brochures, monitoring information, site communication, and trial operations data to spot risks and changes faster.
Create MSL briefings, medical Q&A, congress summaries, literature overviews, and internal knowledge articles — always with sources, versioning, and approval processes.
Connect manufacturing, quality, supply chain, and inventory data to better understand shortages, deviations, supplier risks, and product-availability impact.
Built for pharma systems — not just office workflows.
AI in pharma has to work where regulated decisions are made. North connects to the system categories that drive research, quality, regulatory, safety, manufacturing, and medical communication — with sovereign deployment options for sensitive company, patient, and product data.
Instead of switching between document management, QMS, RIM, safety, clinical, LIMS, ERP, and data warehouse systems, employees can ask targeted questions and get traceable answers — grounded in the systems and documents that run regulated operations.
Pharma context
A single conversation can connect scientific evidence, regulatory history, quality events, SOPs, and a recommended action.
Instead of switching between document management, QMS, RIM, safety, clinical, LIMS, ERP, and data warehouse systems, employees can ask targeted questions and get traceable answers — grounded in the systems and documents that run regulated operations.
Regulatory intelligence
RIM + Regulatory DMS + Labeling
Navigate registration dossiers, variations, labeling changes, authority questions, and regulatory commitments.
Quality & compliance intelligence
QMS + eDMS + Training Systems
Analyze SOPs, deviations, CAPAs, change controls, audit findings, training status, and quality risk assessments.
Sovereign by design.
North is designed for pharma and life-sciences companies that work with sensitive research, patient, quality, manufacturing, safety, and regulatory data — and want to adopt AI without giving up control over data, governance, or infrastructure.
Note: Cohere helps companies build controlled, auditable, and sovereign AI workflows. Concrete regulatory assessment, validation, and release remain dependent on the use case, system architecture, and internal quality processes.
EU AI Act ready
Transparency, human oversight, risk classification, and governance controls can be built into workflows so AI is used responsibly in regulated pharma and life-sciences processes.
Air-gapped & hybrid deployment
Run Cohere in the environment that meets your security, compliance, and data-residency requirements — from private cloud to hybrid architectures to fully isolated air-gapped deployments.
Audit-grade traceability
Answers, recommendations, data sources, approvals, and actions are documented so teams can review decisions and meet regulatory or internal requirements.
GxP & Data Integrity — controlled, documented workflows
Cohere supports GxP-oriented ways of working through source citation, role permissions, logging, versioning, and approvals. Teams can embed AI-supported analyses and drafts into existing quality systems and data-integrity principles.
GDPR — Protection of health and personal data
Cohere supports controlled processing of sensitive personal data through private deployments, role-based access, data-residency options, and limiting unnecessary data sharing.
NIS2 — Cybersecurity and resilience
Cohere supports secure and resilient AI workflows through controlled deployments, access controls, logging, and governance for agents that interact with business-critical pharma, manufacturing, quality, and supply-chain systems.
21 CFR Part 11 & Annex 11 — electronic records and controlled systems
Cohere can be embedded into validated system landscapes where electronic records, approvals, user rights, audit trails, and controlled changes are managed with full traceability.
Pharmacovigilance & Medical Information Governance
AI workflows can be designed so safety-relevant information, case summaries, literature signals, and medical answer drafts remain reviewable and are professionally approved before use or communication.
Tailored demo
Define your first sovereign pharma AI workflow.
Talk to Cohere about a demo tailored to your systems, data landscape, and governance requirements. We shape the session around concrete pharma challenges — from Regulatory Affairs and Quality to Medical Affairs, Clinical Operations, Pharmacovigilance, and Manufacturing.
- For Regulatory Affairs, Quality, Medical Affairs, Clinical Operations, Pharmacovigilance, Manufacturing, and Supply Chain.
- For CIO, CDO, CTO, Data, Security, and Compliance teams introducing AI under sovereign and regulated conditions.
- For pharma and life-sciences companies that want to integrate agentic AI safely, under control, and with clear value into existing workflows.