Life sciences
Innovate faster with one regulated AI platform
Securely power life sciences workflows with any AI agent
Life sciences organizations are working with research, clinical, commercial, and manufacturing content — but most of its value remains untapped and underutilized. Box empowers teams to build and govern content-centric processes with any AI agent on a single, GxP-compliant platform. With AI-native workflows, 21 CFR Part 11 e-signatures, and large-scale metadata extraction, you can extract insights and automate processes across the entire life sciences value chain. See why 2,500+ life sciences customers trust Box.
Comply with critical regulations
Enforce retention policies, maintain inspection-ready audit trails, and govern regulated and non-regulated content on a single compliant platform. Box supports GxP Validation with certified partners to deliver environments that meet FDA, GxP, GDPR, HIPAA, DICOM, and 21 CFR Part 11 compliance requirements.
Fast track workflows with AI
90% of data is unstructured. With Box AI, you can use that content to automate research, clinical, quality, and commercial processes. Fuel workflows with custom, no-code AI agents in Box AI Studio, and maintain GxP compliance with built-in governance and AI that doesn’t train on (or autonomously modify) your data.
Achieve greater success with fewer tools
Eliminate point solutions for e-signatures, forms, ECM, and document generation, and reduce IT sprawl and overhead. Enjoy unlimited storage for high content volumes across regulated and non-regulated workflows, and leverage 1,500+ integrations, plus a robust developer platform.
Speed up clinical study startup
Streamline site feasibility, qualification, and activation with automated document routing, 21 CFR Part 11 compliant e-signatures, and secure sponsor-CRO-site collaboration — all in one platform. Box centralizes site feasibility surveys, FDA 1572 forms, Informed Consent Files, and Investigator Brochures, with AI-powered data extraction to qualify sites faster without increasing headcount.
Streamline and secure FDA-compliant e-signatures
Transform signature and approval workflows, from clinical trial enrollment and new drug applications to R&D documentation and manufacturing. GxP customers leverage unlimited, native e-signatures for 21 CFR Part 11 compliance at no additional cost — avoiding the high costs associated with standalone e-signature providers.
Power life science manufacturing from one place
Give manufacturing sites and quality reviewers secure access to batch records in a GMP-compliant platform built for life sciences manufacturing. Stay audit-ready with controlled collaboration, metadata-driven workflows, and compliant e-signatures.
One regulated workflow platform for life sciences
Clinical study startup
Automate site feasibility, qualification, and activation with AI-powered document routing, e-signatures, and free external collaboration.
M&A post-merger integration
Accelerate M&A and PMI cycle times with faster ingestion of R&D data. Seamlessly transition terabytes of regulated content
Promotional materials (MLR review)
Accelerate promotional content approval with automated routing to medical, legal, and regulatory reviewers, real-time status tracking, and compliant 2253 filing.
CRO and CDMO collaboration
Increase control and coordination with CROs, CMOs, and sponsors on a single governed platform.
GMP manufacturing & tech transfer
Digitize batch records and streamline technology transfer with governed workflows, compliant 21 CFR Part 11 sign-off, controlled collaboration, and audit traceability.
Electronic Trial Master Files (eTMF)
Centralize and automate eTMF management with automated structure creation, tracking, and inspection-ready audit trails
Intelligent Content Management across your value chain
Research
Accelerate scientific discovery by centralizing research protocols, lab data, and study submissions on a secure, AI-powered platform with compliant external collaboration
Clinical
Automate clinical study startup, eTMF management, and sponsor-CRO collaboration with AI-powered workflows and free external users.
Manufacturing
Digitize batch records, automate GMP quality workflows, and streamline CMC tech transfer with governed workflows, compliant approvals, and end-to-end traceability.
Commercial
Get therapies to market faster by automating MLR review cycles, centralizing promotional content, and enabling compliant collaboration across agencies and field teams.